TWI727104B

TWI727104B - Wafer laminated body and manufacturing method thereof

Info

Publication number: TWI727104B
Application number: TW106134493A
Authority: TW
Inventors: 安田浩之; 菅生道博; 加藤英人
Original assignee: 日商信越化學工業股份有限公司
Priority date: 2016-10-11
Filing date: 2017-10-06
Publication date: 2021-05-11
Also published as: CN107919315A; EP3309824A1; JP6614090B2; CN107919315B; KR20180040093A; KR102443881B1; JP2018063972A; US10553552B2; US20180102334A1; EP3309824B1; TW201828329A

Abstract

本發明之課題為提供支持體與晶圓之接合容易，晶圓自支持體之剝離亦容易，且可提高薄型晶圓之生產性，適於薄型晶圓製造的晶圓層合體，及其製造方法。　　其解決手段為一種晶圓層合體，其係具備支持體、形成於該支持體上之接著劑層、與於該接著劑層以具有電路面之表面呈對向的方式層合之晶圓的晶圓層合體，其中前述接著劑層，自前述支持體側起，係依序由具有遮光性之樹脂層A，與含有非聚矽氧系熱可塑性樹脂之樹脂層B所構成，樹脂層A含有包含含有縮合環之重複單位的樹脂，且樹脂層B，於25℃之儲存模數E’為1~500MPa，且拉伸斷裂強度為5~50MPa。The subject of the present invention is to provide easy bonding between a support and a wafer, and easy peeling of the wafer from the support, and can improve the productivity of thin wafers, a wafer laminate suitable for thin wafer manufacturing, and its production method. The solution is a wafer laminate, which is provided with a support, an adhesive layer formed on the support, and a wafer laminated on the adhesive layer with a circuit surface facing the surface A wafer laminate, wherein the adhesive layer is composed of a resin layer A with light-shielding properties and a resin layer B containing a non-silicone thermoplastic resin in order from the support side, and the resin layer A It contains a resin containing a repeating unit containing a condensed ring, and the storage modulus E'of the resin layer B at 25° C. is 1 to 500 MPa, and the tensile breaking strength is 5 to 50 MPa.

Description

Wafer laminated body and manufacturing method thereof

[0001] 本發明係關於半導體領域中之晶圓層合體及其製造方法。[0001] The present invention relates to a wafer laminate in the semiconductor field and a manufacturing method thereof.

[0002] 為了實現更加高密度、大容量化，3次元之半導體構裝正成為必須。3次元構裝技術，係指將1個半導體晶片薄型化，進而將其以矽貫通電極(TSV：through silicon via)結線，同時層合為多層之半導體製作技術。為了將其實現，必須有將形成有半導體電路之基板藉由非電路形成面(亦稱為「背面」)研削而薄型化，進一步對背面進行形成含有TSV之電極的步驟。以往，矽基板之背面研削步驟中，係於研削面之相反側貼上背面保護膠帶，防止研削時之晶圓破損。但是，該膠帶係將有機樹脂薄膜使用於支持基材，雖具柔軟性，但另一方面，強度或耐熱性不充分，不適於進行TSV形成步驟或於背面之配線層形成步驟。　　[0003] 因而，提出有藉由將半導體基板隔著接著層而接合於矽、玻璃等之支持體，而可充份耐受背面研削、TSV或背面電極形成之步驟的系統。此時重要的是將基板接合於支持體時的接著層。此係以可將基板無間隙地接合於支持體，耐受之後步驟的程度之充分耐久性為必要，且以最後可將薄型晶圓簡便地由支持體剝離為必要。如此地，由於最後會剝離，故本說明書中，將該接著層稱為臨時接著層(或臨時接著劑層)。　　[0004] 至今為止公知之臨時接著層與其剝離方法，提出有將熱熔融性之烴系化合物使用於接著劑，於加熱熔融狀態進行接合/剝離之技術(專利文獻1)。但是，係僅以加熱控制，故簡便但另一方面於超過200℃之高溫下的熱穩定性不充分，因此應用範圍窄。　　[0005] 又，提出有將聚矽氧黏著劑使用於臨時接著劑層之技術(專利文獻2)。此係使用加成硬化型之聚矽氧黏著劑將基板接合於支持體，剝離時浸漬於會溶解或分解聚矽氧樹脂之藥劑而將基板由支持體分離者。因此，剝離需要非常長時間，對實際製造製程之應用困難。　　[0006] 另一方面，亦提出有對含有光吸收性物質之接著劑照射高強度之光，使接著劑層分解，藉以將接著劑層由支持體剝離之技術(專利文獻3)。以該方法雖有將基板由支持體分離時每1枚基板之處理時間短的優點，但由於將所照射之光轉換為熱，因此必須使用金屬化合物，有對基板之金屬污染之虞。 [先前技術文獻] [專利文獻] 　　[0007] 　　[專利文獻1] 日本特開2003-177528號公報　　[專利文獻2] 國際公開第2015/072418號　　[專利文獻3] 日本特開2013-534721號公報[0002] In order to achieve higher density and higher capacity, 3-dimensional semiconductor packaging is becoming necessary. Three-dimensional packaging technology refers to the thinning of a semiconductor wafer, and then connect it with through silicon via (TSV), and laminate it into a multilayer semiconductor manufacturing technology at the same time. In order to realize this, it is necessary to reduce the thickness of the substrate on which the semiconductor circuit is formed by grinding the non-circuit forming surface (also referred to as the "back surface"), and further process the step of forming TSV-containing electrodes on the back surface. In the past, in the back grinding step of the silicon substrate, a back protection tape was attached to the opposite side of the grinding surface to prevent wafer damage during grinding. However, this adhesive tape uses an organic resin film for a supporting substrate. Although it has flexibility, it has insufficient strength and heat resistance and is not suitable for TSV formation steps or wiring layer formation steps on the back surface.　　[0003] Therefore, there is proposed a system that can sufficiently withstand the steps of back grinding, TSV, or back electrode formation by bonding a semiconductor substrate to a support such as silicon or glass via an adhesive layer. What is important here is the adhesive layer when bonding the substrate to the support. This requires that the substrate can be bonded to the support without gaps, and sufficient durability to withstand subsequent steps is necessary, and it is necessary that the thin wafer can be easily peeled from the support at the end. In this way, since it will peel off at the end, this adhesive layer is referred to as a temporary adhesive layer (or temporary adhesive layer) in this specification.　　[0004] The conventionally known temporary adhesive layer and its peeling method have proposed a technique of using a hot-melt hydrocarbon-based compound as an adhesive to perform bonding/peeling in a heat-melted state (Patent Document 1). However, it is only controlled by heating, so it is simple, but on the other hand, the thermal stability at a high temperature exceeding 200°C is not sufficient, so the application range is narrow.　　[0005] In addition, a technique of using a silicone adhesive for a temporary adhesive layer has been proposed (Patent Document 2). This is a method that uses an addition-curing silicone adhesive to join the substrate to the support, and when peeling off, it is immersed in an agent that dissolves or decomposes the silicone resin to separate the substrate from the support. Therefore, peeling takes a very long time, and it is difficult to apply to the actual manufacturing process.　　[0006] On the other hand, a technique of irradiating an adhesive containing a light-absorbing substance with high-intensity light to decompose the adhesive layer to peel the adhesive layer from the support has also been proposed (Patent Document 3). Although this method has the advantage that the processing time per substrate is short when the substrate is separated from the support, but since the irradiated light is converted into heat, a metal compound must be used, which may cause metal contamination of the substrate. [Prior Art Document] [Patent Document] 　　[0007] 　　[Patent Document 1] Japanese Patent Application Publication No. 2003-177528 　　[Patent Document 2] International Publication No. 2015/072418 　　[Patent Document 3] Japanese Patent Application Publication No. 2013-534721

[發明所欲解決之課題] 　　[0008] 本發明係有鑑於前述問題點而為者，其目的為提供支持體與晶圓之接合容易，且亦能夠以高階差基板之均勻膜厚形成，對TSV形成、晶圓背面配線步驟之步驟適合性高，進而CVD(化學氣相成長)等晶圓熱製程耐性優良，晶圓亦容易由支持體剝離，可提高薄型晶圓之生產性的適於薄型晶圓製造之晶圓層合體，及其製造方法。 [用以解決課題之手段] 　　[0009] 本發明者等人為了達成前述目的而進行努力探討的結果，發現藉著藉由將支持體與晶圓使用特定之接著劑層接合而得到之晶圓層合體，可達成前述目的，而完成本發明。　　[0010] 因此，本發明係提供下述晶圓層合體及其製造方法。　　1.一種晶圓層合體，其係具備支持體、形成於該支持體上之接著劑層，與於該接著劑層以具有電路面之表面呈對向的方式層合之晶圓的晶圓層合體，　　前述接著劑層，自前述支持體側起，係依序由具有遮光性之樹脂層A，及含有非聚矽氧系熱可塑性樹脂之樹脂層B所構成，　　樹脂層A，於主鏈含有包含縮合環之樹脂，　　樹脂層B，於25℃之儲存模數E’為1~500MPa，且拉伸斷裂強度為5~50MPa。　　2.如1之晶圓層合體，其中前述非聚矽氧系熱可塑性樹脂，為玻璃轉移溫度-80~120℃之樹脂。　　3.如1或2之晶圓層合體，其中樹脂層A之波長355nm之光的透過率為20%以下。　　4.如1~3中任一項之晶圓層合體，其中樹脂層A為由樹脂組成物A之硬化物所構成者，該樹脂組成物A含有包含下述式(1)表示之重複單位，且重量平均分子量500~ 500,000之樹脂A；

(式中，R¹ ~R³ 係分別獨立地為氫原子、羥基或碳數1~20之1價有機基，但R¹ ~R³ 之至少1者為羥基；R⁴ 為氫原子或可具有取代基之碳數1~30之1價有機基)。　　5.如4之晶圓層合體，其中樹脂組成物A進一步含有交聯劑。　　6.如4或5之晶圓層合體，其中樹脂組成物A進一步含有酸產生劑。　　7.如4~6中任一項之晶圓層合體，其中樹脂組成物A進一步含有有機溶劑。　　8.一種晶圓層合體之製造方法，其係如1~7中任一項之晶圓層合體之製造方法，其包含　　(a)於支持體直接形成樹脂層A之步驟、　　(b)於晶圓之電路形成面形成樹脂層B之步驟，及　　(c)將樹脂層A與樹脂層B於減壓下接合之步驟。　　9.一種晶圓層合體之製造方法，其係如1~7中任一項之晶圓層合體之製造方法，其包含　　(a’)於支持體直接形成樹脂層A形成用之樹脂組成物層A’之步驟、　　(b)於晶圓之電路形成面形成樹脂層B之步驟、　　(c)將樹脂組成物A’與樹脂層B於減壓下接合之步驟，及　　(d)進行熱硬化形成樹脂層A而進行接合之步驟。　　10.一種晶圓層合體之製造方法，其係如1~7中任一項之晶圓層合體之製造方法，其包含　　(a)於支持體直接形成樹脂層A之步驟、　　(b’)於前述樹脂層A之上形成樹脂層B之步驟，及　　(c’)將前述支持體上之樹脂層B與晶圓之電路形成面於減壓下接合之步驟。　　11.一種晶圓層合體之製造方法，其係如1~7中任一項之晶圓層合體之製造方法，其包含　　(a’)於支持體直接形成樹脂層A形成用之樹脂組成物層A’之步驟、　　(b’)於前述樹脂組成物層A’之上形成樹脂層B之步驟、　　(c’)將前述支持體上之樹脂層B與晶圓之電路形成面於減壓下接合之步驟，及　　(d)進行熱硬化形成樹脂層A而進行接合之步驟。　　12.一種薄型晶圓之製造方法，其包含將以如8~11中任一項之方法所得到之晶圓層合體的晶圓之電路非形成面予以研削或研磨之步驟。　　[0011] 依照本發明，可提供在將支持體-晶圓堅固地接合而支持的同時，具有熱耐性，可將晶圓由支持體容易地分離之晶圓層合體。[Problem to be Solved by the Invention] [0008] The present invention is made in view of the aforementioned problems, and its purpose is to provide easy bonding of the support and the wafer, and can also be formed with a uniform film thickness of a high-level difference substrate. The steps of TSV formation and backside wiring of the wafer are highly compatible, and the wafer thermal process resistance such as CVD (Chemical Vapor Growth) is excellent, and the wafer is easily peeled from the support, which can improve the productivity of thin wafers. Wafer laminated body for thin wafer manufacturing, and manufacturing method thereof. [Means for Solving the Problem] [0009] As a result of diligent research in order to achieve the aforementioned object, the inventors found that a wafer obtained by bonding a support and a wafer using a specific adhesive layer The laminated body can achieve the aforementioned objects and complete the present invention. [0010] Therefore, the present invention provides the following wafer laminate and a manufacturing method thereof. 1. A wafer laminate, which is a wafer provided with a support, an adhesive layer formed on the support, and a wafer laminated on the adhesive layer with a circuit surface facing the surface Laminated body, the aforementioned adhesive layer, starting from the aforementioned support side, is composed of a resin layer A with light-shielding properties and a resin layer B containing a non-silicone thermoplastic resin. The resin layer A is in the main The chain contains a resin containing a condensed ring, the resin layer B has a storage modulus E'at 25°C of 1 to 500 MPa, and a tensile breaking strength of 5 to 50 MPa. 2. The wafer laminate as in 1, wherein the aforementioned non-silicone-based thermoplastic resin is a resin with a glass transition temperature of -80~120°C. 3. The wafer laminate of 1 or 2, wherein the light transmittance of the resin layer A with a wavelength of 355nm is 20% or less. 4. The wafer laminate according to any one of 1 to 3, wherein the resin layer A is composed of a cured product of the resin composition A, and the resin composition A contains a repeating unit represented by the following formula (1) , And resin A with a weight average molecular weight of 500~500,000;

(In the formula, R ¹ to R ³ are each independently a hydrogen atom, a hydroxyl group or a monovalent organic group with 1 to 20 carbons, but ^{at least one of R 1} to R ³ is a hydroxyl group; R ⁴ is a hydrogen atom or may Substituent monovalent organic group with 1 to 30 carbons). 5. The wafer laminate according to 4, wherein the resin composition A further contains a crosslinking agent. 6. The wafer laminate according to 4 or 5, wherein the resin composition A further contains an acid generator. 7. The wafer laminate according to any one of 4 to 6, wherein the resin composition A further contains an organic solvent. 8. A method of manufacturing a wafer laminate, which is the method of manufacturing a wafer laminate according to any one of 1 to 7, which includes (a) the step of directly forming the resin layer A on the support, (b) in The step of forming the resin layer B on the circuit formation surface of the wafer, and (c) the step of bonding the resin layer A and the resin layer B under reduced pressure. 9. A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of 1 to 7, which includes (a') directly forming a resin composition for forming a resin layer A on a support The step of layer A', (b) the step of forming the resin layer B on the circuit formation surface of the wafer, (c) the step of bonding the resin composition A'and the resin layer B under reduced pressure, and (d) heat The step of hardening to form the resin layer A and joining. 10. A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of 1 to 7, which includes (a) the step of directly forming the resin layer A on the support, (b') A step of forming a resin layer B on the aforementioned resin layer A, and (c') a step of joining the resin layer B on the aforementioned support to the circuit forming surface of the wafer under reduced pressure. 11. A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of 1 to 7, which includes (a') directly forming a resin composition for forming a resin layer A on a support The step of layer A', (b') the step of forming the resin layer B on the resin composition layer A', (c') the resin layer B on the support and the circuit forming surface of the wafer at a reduced pressure The next step of bonding, and (d) the step of thermosetting to form the resin layer A and bonding. 12. A method of manufacturing a thin wafer, which includes the step of grinding or polishing the circuit non-forming surface of the wafer of the wafer laminate obtained by the method of any one of 8-11. [0011] According to the present invention, it is possible to provide a wafer laminate body that has heat resistance while firmly bonding and supporting the support-wafer, and can easily separate the wafer from the support.

[0013] 本發明之晶圓層合體，為具備支持體、形成於該支持體上之接著劑層，與於該接著劑層以具有電路面之表面呈對向的方式層合之晶圓的晶圓層合體。前述接著劑層，自前述支持體側起，係依序由具有遮光性之樹脂層A，及含有非聚矽氧系熱可塑性樹脂之樹脂層B所構成。　　[0014] 具體說明本發明之晶圓層合體之構造，例如，如圖1所示，為支持體1與晶圓3以接著劑層2接合者。接著劑層2，為由鄰接於支持體1所形成之樹脂層2a，與鄰接於樹脂層2a所形成之樹脂層2b的2層所構成者。　　[0015] [支持體] 　　前述支持體，可列舉透明基板、矽晶圓、陶瓷基板等，就剝離支持體時所照射之雷射的透過性觀點而言，較佳為透明基板。前述透明基板，通常可使用玻璃基板或石英基板，其厚度通常較佳為300~1,000μm、更佳為500~ 800μm。　　[0016] [晶圓] 　　前述晶圓，通常為半導體晶圓。該半導體晶圓之例子，可列舉矽晶圓、鍺晶圓、鎵-砷晶圓、鎵-磷晶圓、鎵-砷-鋁晶圓等。前述晶圓之厚度並無特殊限定，通常較佳為600~800μm、更佳為625~775μm。　　[0017] [樹脂層A] 　　樹脂層A為含有於主鏈包含縮合環之樹脂者，其係具有遮光性之樹脂層(遮光層)，波長355nm之光的透過率較佳為20%以下、更佳為18%以下、又更佳為15%以下。又，樹脂層A，吸收極大波長較佳為300~500nm、更佳為300~400nm。進一步地，樹脂層A，波長300~500nm之光的透過率較佳為20%以下。　　[0018] 由耐熱性、接著性、耐藥品性等之觀點而言，樹脂層A中所含有的樹脂，較佳為由樹脂組成物A之硬化物所構成者，該樹脂組成物A含有包含下述式(1)表示之重複單位之樹脂A。式(1)表示之重複單位，可僅含有1種、亦可含有2種以上。

[0019] 式(1)中，R¹ ~R³ ，係分別獨立地為氫原子、羥基，或碳數1~20、較佳為碳數1~10之1價有機基。惟，R¹ ~R³ 之至少1者為羥基。　　[0020] 前述1價有機基，可列舉甲基、乙基、n-丙基、異丙基、n-丁基、sec-丁基、tert-丁基、n-戊基、新戊基、n-己基、n-庚基、n-辛基、n-壬基、n-癸基、n-十二烷基、n-十五烷基、n-二十烷基、環戊基、環己基、環戊基甲基、環己基甲基、環戊基乙基、環己基乙基、環戊基丁基、環己基丁基、金剛烷基等之直鏈狀、分支狀或環狀之碳數1~20之烷基；甲氧基等之直鏈狀、分支狀或環狀之碳數1~5之烷氧基；環氧丙氧基等之含環氧基之基；苯基、萘基等之芳基等。R¹ ~R³ ，較佳為氫原子、羥基、甲基等。　　[0021] 式(1)中，R⁴ 為氫原子，或可具有取代基之碳數1~30、較佳為碳數1~10之1價有機基。R⁴ 表示之1價有機基，可列舉烷基、苯基、萘基、蒽基、降莰基等，此等之氫原子之一部分，亦可經烷基、芳基、醛基、鹵素原子、硝基、腈基、羥基等取代。　　[0022] 樹脂A，通常可藉由於無溶劑或溶劑中使用酸或鹼作為觸媒，於室溫或依需要之冷卻或加熱下，使萘酚或其衍生物與醛化合物進行聚縮合反應而得到。　　[0023] 前述萘酚或其衍生物，可列舉1-萘酚、2-萘酚、2-甲基-1-萘酚、4-甲氧基-1-萘酚、7-甲氧基-2-萘酚、1,2-二羥基萘、1,3-二羥基萘、2,3-二羥基萘、1,4-二羥基萘、1,5-二羥基萘、1,6-二羥基萘、2,6-二羥基萘、1,7-二羥基萘、2,7-二羥基萘、1,8-二羥基萘、5-胺基-1-萘酚、2-甲氧基羰基-1-萘酚、1-(4-羥基苯基)萘、6-(4-羥基苯基)-2-萘酚、6-(環己基)-2-萘酚、1,1’-聯-2-萘酚、6,6’-聯-2-萘酚、9,9-雙(6-羥基-2-萘基)茀、6-羥基-2-乙烯基萘、1-羥基甲基萘、2-羥基甲基萘等。前述萘酚或其衍生物，可1種單獨或組合2種以上使用。　　[0024] 前述醛化合物，可列舉下述式(2)表示者。　　R⁴ -CHO (2) 　　(式中，R⁴ 係與前述相同)。　　[0025] 式(2)表示之醛化合物，例如可列舉甲醛、三噁烷、多聚甲醛、乙醛、丙醛、金剛烷甲醛、苯甲醛、苯基乙醛、α-苯基丙醛、β-苯基丙醛、o-氯苯甲醛、m-氯苯甲醛、p-氯苯甲醛、o-硝基苯甲醛、m-硝基苯甲醛、p-硝基苯甲醛、o-甲基苯甲醛、m-甲基苯甲醛、p-甲基苯甲醛、p-乙基苯甲醛、p-n-丁基苯甲醛、1-萘醛、2-萘醛、蒽甲醛、芘甲醛、糠醛、二甲縮醛、鄰苯二甲醛、間苯二甲醛、對苯二甲醛、萘二甲醛、蒽二甲醛、芘二甲醛等。前述醛化合物，可1種單獨或組合2種以上使用。　　[0026] 前述聚縮合反應所用之溶劑，例如可列舉甲醇、乙醇、異丙醇、丁醇、乙二醇、丙二醇、二乙二醇、甘油、甲基賽珞蘇、乙基賽珞蘇、丁基賽珞蘇、丙二醇單甲基醚等之醇類；二乙基醚、二丁基醚、二乙二醇二乙基醚、二乙二醇二甲基醚、四氫呋喃(THF)、1,4-二噁烷等之醚類；二氯甲烷、氯仿、二氯乙烷、三氯乙烯等之氯系溶劑；己烷、庚烷、苯、甲苯、二甲苯、異丙苯等之烴類；乙腈等之腈類；丙酮、乙基甲基酮、異丁基甲基酮等之酮類；乙酸乙酯、乙酸n-丁酯、丙二醇甲基醚乙酸酯等之酯類；γ-丁內酯等之內酯類；二甲基亞碸、N,N-二甲基甲醯胺、六甲基磷三醯胺等之非質子性極性溶劑。此等溶劑可1種單獨或混合2種以上使用。此等之溶劑，相對於萘酚或其衍生物與醛化合物之合計100質量份而言，較佳可於0~2,000質量份、更佳可於10~2,000質量份之範圍使用。　　[0027] 前述聚縮合反應所用之酸觸媒，例如可列舉鹽酸、溴化氫酸、硫酸、硝酸、磷酸、雜多酸等之無機酸類；草酸、三氟乙酸、甲烷磺酸、苯磺酸、p-甲苯磺酸、三氟甲烷磺酸等之有機酸類；三氯化鋁、乙氧化鋁、異丙氧化鋁、三氟化硼、三氯化硼、三溴化硼、四氯化錫、四溴化錫、二氯化二丁基錫、二甲氧化二丁基錫、氧化二丁基錫、四氯化鈦、四溴化鈦、甲氧化鈦(IV)、乙氧化鈦(IV)、異丙氧化鈦(IV)、氧化鈦(IV)等之路易士酸類。　　[0028] 又，前述聚縮合反應所用之鹼觸媒，例如可列舉氫氧化鈉、氫氧化鉀、氫氧化鋇、碳酸鈉、碳酸氫鈉、碳酸鉀、氫化鋰、氫化鈉、氫化鉀、氫化鈣等之無機鹼類；甲基鋰、n-丁基鋰、氯化甲基鎂、溴化乙基鎂等之烷基金屬類；甲氧化鈉、乙氧化鈉、tert-丁氧化鉀等之烷氧化物類；三乙胺、二異丙基乙胺、N,N-二甲基苯胺、吡啶、4-二甲基胺基吡啶等之有機鹼類。　　[0029] 觸媒之使用量，相對於萘酚或其衍生物與醛化合物之合計100質量份而言，較佳為0.001~100質量份、更佳為0.005~50質量份之範圍。反應溫度較佳為-50℃至溶劑之沸點左右、更佳為室溫至100℃。　　[0030] 聚縮合反應方法，可列舉將萘酚或其衍生物、醛類、觸媒一次給料之方法，或於觸媒存在下滴下萘酚或其衍生物、醛類之方法。　　[0031] 萘酚或其衍生物與醛化合物之使用比率，相對於萘酚或其衍生物之合計而言，醛化合物以莫耳比計，較佳為0.01~5、更佳為0.05~2、又更佳為0.05~1、最佳為0.1~0.9。　　[0032] 聚縮合反應結束後，為了去除系內所存在之未反應原料、觸媒等，可將反應釜之溫度上昇至130~230℃，以1~50mmHg左右將揮發成分去除，或添加適當的溶劑或水將聚合物區分，或將聚合物溶解於良溶劑後於不良溶劑中再沈澱。此等可依所得反應生成物之性質來分別使用。　　[0033] 樹脂A之重量平均分子量(Mw)，較佳為500~ 500,000、更佳為1,000~100,000。前述聚合物之分散度，較佳為1.2~20之範圍，若將單體成分、寡聚物成分或Mw未達500之低分子量體去除時，可抑制烘烤中之揮發成分，可防止烘烤杯周邊之污染或揮發成分之落下所致的表面缺陷產生。再者，本發明中，Mw，係指以使用THF作為溶劑之凝膠滲透層析(GPC)所得的聚苯乙烯換算測定值。　　[0034] 樹脂組成物A，較佳為含有將樹脂A藉由熱反應而交聯之交聯劑。前述交聯劑，適合使用分子內具有2個以上之官能基的環氧化合物、環氧樹脂、羥甲基三聚氰胺等之胺基樹脂等，為了促進此等交聯劑與前述聚合物之交聯反應，較佳為進一步添加觸媒。　　[0035] 前述環氧化合物或環氧樹脂，可列舉2官能、3官能、4官能以上之多官能環氧樹脂，例如日本化藥(股)製之EOCN-1020(參照下述式)、EOCN-102S、XD-1000、NC-2000-L、EPPN-201、GAN、NC6000，或下述式表示者等。　　[0036]

[0037] 使用前述環氧化合物或環氧樹脂作為交聯劑時，其摻合量，相對於具有式(1)表示之重複單位的聚合物100質量份而言，較佳為0.1~50質量份、更佳為0.1~30質量份、又更佳為1~30質量份。交聯劑，可1種單獨或組合2種以上使用。摻合量若為前述範圍，則可得到充分之交聯密度，所得之硬化物會充分發揮功能。　　[0038] 再者，使用前述環氧樹脂作為交聯劑時，較佳為添加硬化促進劑作為觸媒。藉由含有環氧樹脂硬化促進劑，可適切且均勻地進行硬化反應。　　[0039] 環氧樹脂硬化促進劑，例如可列舉2-甲基咪唑、2-乙基咪唑、2-乙基-4-甲基咪唑，及此等化合物之異氰酸乙酯化合物；2-苯基咪唑、2-苯基-4-甲基咪唑、2-苯基-4-甲基-5-羥基甲基咪唑、2-苯基-4,5-二羥基甲基咪唑等之咪唑化合物；1,8-二氮雜雙環[5.4.0]十一烯-7(DBU)、1,5-二氮雜雙環[4.3.0]壬烯-5(DBN)、DBU之有機酸鹽、DBU之酚樹脂鹽、DBU衍生物之四苯基硼酸鹽等之DBU系化合物；三苯基膦、三丁基膦、參(p-甲基苯基)膦、參(p-甲氧基苯基)膦、參(p-乙氧基苯基)膦、三苯基膦/硼酸三苯酯、四苯基膦/四苯基硼酸鹽等之三有機膦類；4級鏻鹽；三乙銨/硼酸三苯酯等之3級胺、及其四苯基硼酸鹽等。前述環氧樹脂硬化促進劑，可1種單獨使用、亦可合併使用2種以上。　　[0040] 環氧樹脂硬化促進劑之摻合量，相對於樹脂A 100質量份而言，較佳為0.1~10質量份、更佳為0.2~5質量份。　　[0041] 又，本發明中使用之羥甲基三聚氰胺等之胺基樹脂，可列舉選自由經福馬林或福馬林-醇改質之胺基縮合物及1分子中平均具有2個以上之羥甲基或烷氧基羥甲基之酚化合物所成之群的1種以上之化合物。　　[0042] 前述胺基樹脂，較佳為Mw為150~10,000者、更佳為200~3,000者。Mw若為前述範圍，可得到充分之硬化性，組成物之硬化後的耐熱性亦良好。　　[0043] 前述經福馬林或福馬林-醇改質之胺基縮合物，例如可列舉經福馬林或福馬林-醇改質之三聚氰胺縮合物，或經福馬林或福馬林-醇改質之尿素縮合物。　　[0044] 前述經福馬林或福馬林-醇改質之三聚氰胺縮合物，例如可遵照公知之方法將三聚氰胺單體以福馬林羥甲基化而改質，或將其進一步以醇烷氧基化而改質，作為下述式表示之改質三聚氰胺藉以配製。再者，作為前述醇，較佳為低級醇，例如碳數1~4之醇。　　[0045]

(式中，R⁵ ~R¹⁰ ，係分別獨立地為羥甲基；含有直鏈狀、分支狀或環狀之碳數1~4之烷氧基之烷氧基甲基；或氫原子，但至少1者為羥甲基或烷氧基甲基)。　　[0046] 前述改質三聚氰胺，可列舉三甲氧基甲基單羥甲基三聚氰胺、二甲氧基甲基單羥甲基三聚氰胺、三羥甲基三聚氰胺、六羥甲基三聚氰胺、六甲氧基羥甲基三聚氰胺等。接著，藉由將前述改質三聚氰胺或由其所得之多聚體(例如2聚體、3聚體等之寡聚物)遵照一般方法加成縮合聚合至成為甲醛與所期望之分子量為止，可得到經福馬林或福馬林-醇改質之三聚氰胺縮合物。再者，可使用前述改質三聚氰胺及其縮合體之1種以上的改質三聚氰胺縮合物作為交聯劑。　　[0047] 又，經福馬林或福馬林-醇改質之尿素縮合物，例如可藉由遵照公知之方法將所期望之分子量的尿素縮合物以福馬林羥甲基化而改質，或將其進一步以醇烷氧基化而改質來配製。　　[0048] 前述改質尿素縮合物之具體例子，例如可列舉甲氧基甲基化尿素縮合物、乙氧基甲基化尿素縮合物、丙氧基甲基化尿素縮合物等。再者，可使用此等1種以上之改質尿素縮合物。　　[0049] 此等之中，作為1分子中平均具有2個以上之羥甲基或烷氧基羥甲基的酚化合物，例如可列舉(2-羥基-5-甲基)-1,3-苯二甲醇、2,2’,6,6’-四甲氧基甲基雙酚A等。　　[0050] 此等胺基縮合物或酚化合物，可1種單獨或組合2種以上使用。　　[0051] 前述交聯劑之摻合量，相對於樹脂A 100質量份而言，較佳為0.1~50質量份、更佳為1~30質量份。若為前述範圍，則組成物A充分硬化，所得之硬化物會充分發揮功能。　　[0052] 再者，使用前述羥甲基三聚氰胺等之胺基樹脂作為交聯劑時，較佳為添加熱酸產生劑作為觸媒。該熱酸產生劑並無特殊限定，例如可列舉下述式表示之銨鹽。

(式中，R¹¹ ~R¹⁴ ，係分別獨立地表示氫原子；直鏈狀、分支狀或環狀之碳數1~12之烷基或側氧基烷基；直鏈狀、分支狀或環狀之碳數2~12之烯基或側氧基烯基；碳數6~20之芳基；或碳數7~12之芳烷基或芳基側氧基烷基，此等基之氫原子的一部分或全部亦可被烷氧基取代。由R¹¹ ~R¹⁴ 中選出之2者，亦可與此等所鍵結之氮原子一起形成環，該環為環中具有式中之氮原子的碳數3~10之脂肪族環，或環中具有式中之氮原子的碳數5~10之雜芳香族環。X^- 為α位之至少1者被氟化之磺酸、全氟烷基醯亞胺酸或全氟烷基甲基化酸)。　　[0053] X^- 具體而言可列舉三氟甲磺酸陰離子、九氟丁磺酸陰離子等之全氟烷磺酸陰離子；α位之至少1者被氟取代之磺酸陰離子；雙(三氟甲基磺醯基)醯亞胺陰離子、雙(全氟乙基磺醯基)醯亞胺陰離子、雙(全氟丁基磺醯基)醯亞胺陰離子等之醯亞胺陰離子；參(三氟甲基磺醯基)甲基體陰離子、參(全氟乙基磺醯基)甲基體陰離子等之甲基體(methanide)陰離子。　　[0054] 熱酸產生劑之摻合量，相對於樹脂A 100質量份而言，較佳為0.1~15質量份、更佳為0.2~10質量份。若為前述範圍，則組成物A充分硬化，組成物A之保存穩定性亦良好。　　[0055] 樹脂組成物A亦可含有溶劑。前述溶劑例如可列舉環己酮、環戊酮、甲基-2-n-戊基酮等之酮類；3-甲氧基丁醇、3-甲基-3-甲氧基丁醇、1-甲氧基-2-丙醇、1-乙氧基-2-丙醇等之醇類；丙二醇單甲基醚、乙二醇單甲基醚、丙二醇單乙基醚、乙二醇單乙基醚、丙二醇二甲基醚、二乙二醇二甲基醚等之醚類；丙二醇單甲基醚乙酸酯、丙二醇單乙基醚乙酸酯、乳酸乙酯、丙酮酸乙酯、乙酸丁酯、3-甲氧基丙酸甲酯、3-乙氧基丙酸乙酯、乙酸tert-丁酯、丙酸tert-丁酯、丙二醇單-tert-丁基醚乙酸酯、γ-丁內酯等之酯類等。此等可1種單獨或混合2種以上使用。前述溶劑之摻合量，相對於樹脂A 100質量份而言，較佳為100~5,000質量份、更佳為150~2,500質量份。　　[0056] 又，樹脂組成物A，亦可作為不含溶劑之薄膜狀組成物使用。　　[0057] 樹脂組成物A，亦可依需要含有界面活性劑，或以更提高耐熱性為目的含有抗氧化劑等。　　[0058] 界面活性劑並無特殊限定，例如可列舉聚氧乙烯月桂基醚、聚氧乙烯硬脂基醚、聚氧乙烯鯨蠟基醚、聚氧乙烯油基醚等之聚氧乙烯烷基醚類；聚氧乙烯辛基酚醚、聚氧乙烯壬基酚醚等之聚氧乙烯烷基芳基醚類；聚氧乙烯聚氧丙烯嵌段共聚物類；山梨醇酐單月桂酸酯、山梨醇酐單棕櫚酸酯、山梨醇酐單硬脂酸酯等之山梨醇酐脂肪酸酯類；聚氧乙烯山梨醇酐單月桂酸酯、聚氧乙烯山梨醇酐單棕櫚酸酯、聚氧乙烯山梨醇酐單硬脂酸酯、聚氧乙烯山梨醇酐三油酸酯、聚氧乙烯山梨醇酐三硬脂酸酯等之聚氧乙烯山梨醇酐脂肪酸酯之非離子系界面活性劑；Eftop(註冊商標)EF301、EF303、EF352((股)Tokem Products製)、Megafac(註冊商標)F171、F172、F173(DIC(股)製)、Fluorad(註冊商標)FC430、FC431(3M公司製)、Asahiguard AG710、Surflon(註冊商標)S-381、S-382、SC101、SC102、SC103、SC104、SC105、SC106、Sufynol(註冊商標)E1004、KH-10、KH-20、KH-30、KH-40(旭硝子(股))等之氟系界面活性劑；有機矽氧烷聚合物KP341、X-70-092、X-70-093、X-70-1102(信越化學工業(股)製)、丙烯酸系或甲基丙烯酸系POLYFLOW No. 75、No. 95(共榮社化學(股)製)。此等可1種單獨或組合2種以上使用。　　[0059] 抗氧化劑較佳為由受阻酚系化合物、受阻胺系化合物、有機磷化合物及有機硫化合物中選出之至少1種。　　[0060] 前述受阻酚系化合物並無特殊限定，較佳為以下所列舉者。例如可列舉1,3,5-三甲基-2,4,6-參(3,5-二-tert-丁基-4-羥基苄基)苯(商品名：IRGANOX 1330)、2,6-二-tert-丁基-4-甲基酚(商品名：Sumilizer BHT)、2,5-二-tert-丁基-氫醌(商品名：Nocrac NS-7)、2,6-二-tert-丁基-4-乙基酚(商品名：Nocrac M-17)、2,5-二-tert-戊基氫醌(商品名：Nocrac DAH)、2,2’-亞甲基雙(4-甲基-6-tert-丁基酚)(商品名：Nocrac NS-6)、3,5-二-tert-丁基-4-羥基-苄基膦酸酯-二乙基酯(商品名：IRGANOX 1222)、4,4’-硫雙(3-甲基-6-tert-丁基酚)(商品名：Nocrac 300)、2,2’-亞甲基雙(4-乙基-6-tert-丁基酚)(商品名：Nocrac NS-5)、4,4’-亞丁基雙(3-甲基-6-tert-丁基酚)(商品名：ADK STAB AO-40)、2-tert-丁基-6-(3-tert-丁基-2-羥基-5-甲基苄基)-4-甲基苯基丙烯酸酯(商品名：Sumilizer GM)、2-[1-(2-羥基-3,5-二-tert-戊基苯基)乙基]-4,6-二-tert-戊基苯基丙烯酸酯(商品名：Sumilizer GS)、2,2’-亞甲基雙[4-甲基-6-(α-甲基-環己基)酚]、4,4’-亞甲基雙(2,6-二-tert-丁基酚)(商品名：Seenox 226M)、4,6-雙(辛硫基甲基)-o-甲酚(商品名：IRGANOX 1520L)、2,2’-伸乙雙(4,6-二-tert-丁基酚)、十八烷基-3-(3,5-二-tert-丁基-4-羥基苯基)丙酸酯(商品名：IRGANOX 1076)、1,1,3-參-(2-甲基-4-羥基-5-tert-丁基苯基)丁烷(商品名：ADK STAB AO-30)、肆[亞甲基-(3,5-二-tert-丁基-4-羥基氫桂皮酸酯)]甲烷(商品名：ADK STAB AO-60)、三乙二醇雙[3-(3-tert-丁基-5-甲基-4-羥基苯基)丙酸酯](商品名：IRGANOX 245)、2,4-雙-(n-辛硫基)-6-(4-羥基-3,5-二-tert-丁基苯胺基)-1,3,5-三嗪(商品名：IRGANOX 565)、N,N’-六亞甲基雙(3,5-二-tert-丁基-4-羥基-氫桂皮醯胺)(商品名：IRGANOX 1098)、1,6-己二醇-雙[3-(3,5-二-tert-丁基-4-羥基苯基)丙酸酯](商品名：IRGANOX 259)、2,2-硫基-二伸乙雙[3-(3,5-二-tert-丁基-4-羥基苯基)丙酸酯](商品名：IRGANOX 1035)、3,9-雙[2-[3-(3-tert-丁基-4-羥基-5-甲基苯基)丙醯氧基]1,1-二甲基乙基]2,4,8,10-四氧雜螺[5.5]十一烷(商品名：Sumilizer GA-80)、參-(3,5-二-tert-丁基-4-羥基苄基)異三聚氰酸酯(商品名：IRGANOX 3114)、雙(3,5-二-tert-丁基-4-羥基苄基膦酸乙酯)鈣/聚乙烯蠟混合物(50：50)(商品名：IRGANOX 1425WL)、異辛基-3-(3,5-二-tert-丁基-4-羥基苯基)丙酸酯(商品名：IRGANOX 1135)、4,4’-硫基雙(6-tert-丁基-3-甲基酚)(商品名：Sumilizer WX-R)、6-[3-(3-tert-丁基-4-羥基-5-甲基苯基)丙氧基]-2,4,8,10-四-tert-丁基二苯并[d,f][1,3,2]二氧雜磷雜庚英(商品名：Sumilizer GP)等。　　[0061] 前述受阻胺系化合物，並無特殊限定，較佳為以下所列舉者。例如可列舉p,p’-二辛基二苯胺(商品名：IRGANOX 5057)、苯基-α-萘胺(Nocrac PA)、聚(2,2,4-三甲基-1,2-二氫喹啉)(商品名：Nocrac 224、224-S)、6-乙氧基-2,2,4-三甲基-1,2-二氫喹啉(商品名：Nocrac AW)、N,N’-二苯基-p-苯二胺(商品名：Nocrac DP)、N,N’-二-β-萘基-p-苯二胺(商品名：Nocrac White)、N-苯基-N’-異丙基-p-苯二胺(商品名：Nocrac 810NA)、N,N’-二烯丙基-p-苯二胺(商品名：Nonflex TP)、4,4’-(α,α-二甲基苄基)二苯胺(商品名：Nocrac CD)、p,p-甲苯磺醯基胺基二苯胺(商品名：Nocrac TD)、N-苯基-N’-(3-甲基丙烯醯氧基-2-羥基丙基)-p-苯二胺(商品名：Nocrac G1)、N-(1-甲基庚基)-N’-苯基-p-苯二胺(商品名：Ozonon 35)、N,N’-二-sec-丁基-p-苯二胺(商品名：Sumilizer BPA)、N-苯基-N’-1,3-二甲基丁基-p-苯二胺(商品名：Antigene 6C)、烷基化二苯胺(商品名：Sumilizer 9A)、琥珀酸二甲基-1-(2-羥基乙基)-4-羥基-2,2,6,6-四甲基哌啶聚縮合物(商品名：Tinuvin 622LD)、聚[[6-(1,1,3,3-四甲基丁基)胺基-1,3,5-三嗪-2,4-二基][(2,2,6,6-四甲基-4-哌啶基)亞胺基]六亞甲基[(2,2,6,6-四甲基-4-哌啶基)亞胺基]](商品名：CHIMASSORB 944)、N,N’-雙(3-胺基丙基)乙二胺-2,4-雙[N-丁基-N-(1,2,2,6,6-五甲基-4-哌啶基)胺基]-6-氯-1,3,5-三嗪縮合物(商品名：CHIMASSORB 119FL)、雙(1-辛氧基-2,2,6,6-四甲基-4-哌啶基)癸二酸酯(商品名：TINUVIN 123)、雙(2,2,6,6-四甲基-4-哌啶基)癸二酸酯(商品名：TINUVIN 770)、2-(3,5-二-tert-丁基-4-羥基苄基)-2-n-丁基丙二酸雙(1,2,2,6,6-五甲基-4-哌啶基)(商品名：TINUVIN 144)、雙(1,2,2,6,6-五甲基-4-哌啶基)癸二酸酯(商品名：TINUVIN 765)、肆(1,2,2,6,6-五甲基-4-哌啶基)1,2,3,4-丁烷四羧酸酯(商品名：LA-57)、肆(2,2,6,6-四甲基-4-哌啶基)1,2,3,4-丁烷四羧酸酯(商品名：LA-52)、1,2,3,4-丁烷四羧酸與1,2,2,6,6-五甲基-4-哌啶醇及1-十三醇之混合酯化物(商品名：LA-62)、1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-4-哌啶醇及1-十三醇之混合酯化物(商品名：LA-67)、1,2,3,4-丁烷四羧酸與1,2,2,6,6-五甲基-4-哌啶醇及3,9-雙(2-羥基-1,1-二甲基乙基)-2,4,8,10-四氧雜螺[5.5]十一烷之混合酯化物(商品名：LA-63P)、1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-4-哌啶醇及3,9-雙(2-羥基-1,1-二甲基乙基)-2,4,8,10-四氧雜螺[5.5]十一烷之混合酯化物(商品名：LA-68LD)、(2,2,6,6-四亞甲基-4-哌啶基)-2-伸丙基羧酸酯(商品名：ADK STAB LA-82)、(1,2,2,6,6-五甲基-4-哌啶基)-2-伸丙基羧酸酯(商品名：ADK STAB LA-87)等。　　[0062] 前述有機磷化合物，並無特殊限定，較佳為以下所列舉者。例如可列舉雙(2,4-二-tert-丁基苯基)[1,1-聯苯基]-4,4’-二基雙亞磷酸酯、9,10-二氫-9-氧雜-10-磷雜菲-10-氧化物(商品名：SANKO-HCA)、亞磷酸三乙酯(商品名：JP302)、亞磷酸三-n-丁酯(商品名：JP304)、亞磷酸三苯酯(商品名：ADK STAB TPP)、亞磷酸二苯基單辛酯(商品名：ADK STAB C)、三(p-甲酚基)亞磷酸酯(商品名：Chelex-PC)、亞磷酸二苯基單癸酯(商品名：ADK STAB 135A)、二苯基單(十三烷基)亞磷酸酯(商品名：JPM313)、參(2-乙基己基)亞磷酸酯(商品名：JP308)、亞磷酸苯基二癸酯(商品名：ADK STAB 517)、亞磷酸十三烷酯(商品名：ADK STAB 3010)、四苯基二丙二醇二亞磷酸酯(商品名：JPP100)、雙(2,4-二-tert-丁基苯基)季戊四醇二亞磷酸酯(商品名：ADK STAB PEP-24G)、參(十三烷基)亞磷酸酯(商品名：JP333E)、雙(壬基苯基)季戊四醇二亞磷酸酯(商品名：ADK STAB PEP-4C)、雙(2,6-二-tert-丁基-4-甲基苯基)季戊四醇二亞磷酸酯(商品名：ADK STAB PEP-36)、雙[2,4-二(1-苯基異丙基)苯基]季戊四醇二亞磷酸酯(商品名：ADK STAB PEP-45)、三月桂基三硫基亞磷酸酯(商品名：JPS312)、參(2,4-二-tert-丁基苯基)亞磷酸酯(商品名：IRGAFOS 168)、參(壬基苯基)亞磷酸酯(商品名：ADK STAB 1178)、二硬脂基季戊四醇二亞磷酸酯(商品名：ADK STAB PEP-8)、參(單,二壬基苯基)亞磷酸酯(商品名：ADK STAB 329K)、亞磷酸三油酯(商品名：Chelex-OL)、亞磷酸三硬脂酯(商品名：JP318E)、4,4’-亞丁基雙(3-甲基-6-tert-丁基苯基二-十三烷基)亞磷酸酯(商品名：JPH1200)、四(C₁₂ -C₁₅ 混合烷基)-4,4’-異亞丙基二苯基二亞磷酸酯(商品名：ADK STAB 1500)、四(十三烷基)-4,4’-亞丁基雙(3-甲基-6-tert-丁基酚)二亞磷酸酯(商品名：ADK STAB 260)、六(十三烷基)-1,1,3-參(2-甲基-5-tert-丁基-4-羥基苯基)丁烷-三亞磷酸酯(商品名：ADK STAB 522A)、氫化雙酚A亞磷酸酯聚合物(HBP)、肆(2,4-二-tert-丁基苯氧基)4,4’-聯苯烯-二-膦(商品名：P-EPQ)、肆(2,4-二-tert-丁基-5-甲基苯氧基)4,4’-聯苯烯-二-膦(商品名：GSY-101P)、2-[[2,4,8,10-肆(1,1-二甲基乙基)二苯并[d,f][1,3,2]二氧雜磷雜庚英-6-基]氧基]-N,N-雙[2-[[2,4,8,10-肆(1,1-二甲基乙基)二苯并[d,f][1,3,2]二氧雜磷雜庚英-6-基]氧基]-乙基]乙胺(商品名：IRGAFOS 12)、2,2’-亞甲基雙(4,6-二-tert-丁基苯基)辛基亞磷酸酯(商品名：ADK STAB HP-10)等。　　[0063] 前述有機硫化合物，並無特殊限定，較佳為以下所列舉者。例如，可列舉二月桂基-3,3’-硫基二丙酸酯(商品名：Sumilizer TPL-R)、二肉豆蔻基-3,3’-硫基二丙酸酯(商品名：Sumilizer TPM)、二硬脂基-3,3’-硫基二丙酸酯(商品名：Sumilizer TPS)、季戊四醇肆(3-月桂基硫基丙酸酯)(商品名：Sumilizer TP-D)、二-十三烷基-3,3’-硫基二丙酸酯(商品名：Sumilizer TL)、2-巰基苯并咪唑(商品名：Sumilizer MB)、二-十三烷基-3,3’-硫基二丙酸酯(商品名：ADK STAB AO-503A)、1,3,5-參-β-硬脂基硫基丙醯氧基乙基異三聚氰酸酯、3,3’-硫基雙丙酸二-十二烷酯(商品名：IRGANOX PS 800FL)、3,3’-硫基雙丙酸二-十八烷酯(商品名：IRGANOX PS 802FL)等。　　[0064] 前述抗氧化劑之中，尤特佳為肆[亞甲基-(3,5-二-tert-丁基-4-羥基氫桂皮酸酯)]甲烷。前述抗氧化劑之添加量，相對於樹脂A 100質量份而言，較佳為0.5~5質量份、更佳為1~3質量份。若為前述範圍，則可得到充分耐熱效果，亦可得到相溶性。再者，抗氧化劑，可1種單獨或組合2種以上使用。　　[0065] 又，為了更加提高耐熱性，於樹脂組成物A中，相對於樹脂A 100質量份而言，亦可添加50質量份以下之公知之二氧化矽等之填料。　　[0066] 樹脂組成物A為溶液時，藉由旋轉塗佈、輥塗佈、模具塗佈、印刷、浸漬等之方法塗佈於支持體上，依其溶劑之揮發條件，較佳為於80~200℃、更佳為於100~180℃之溫度進行預烘烤，使溶劑揮發，藉以形成樹脂組成物層A’。　　[0067] 另一方面，樹脂組成物A為薄膜狀組成物時，可藉由層合法於支持體上形成樹脂組成物層A’。　　[0068] 於支持體上所形成之樹脂組成物層A’，藉由進一步加熱硬化，而作為樹脂層A發揮功能。加熱硬化可藉由加熱板或烘箱進行，其條件，通常係100~350℃、5~10分鐘，較適宜為150~300℃、3~8分鐘。該硬化反應，藉由不使樹脂組成物層A’硬化，形成未硬化狀態之晶圓層合體後，將層合體全體加熱亦會達成。　　[0069] 於支持體上所形成之樹脂層A的膜厚，較佳為0.1~50μm、更佳為0.3~30μm。膜厚若為前述範圍，則遮光性充分，膜之平坦性亦良好。　　[0070] [樹脂層B] 　　樹脂層B，係於25℃之儲存模數E’為1~500MPa，且拉伸斷裂強度為5~50MPa者。E’未達1MPa時，於樹脂層B之背面研削時有產生晶圓之剝離之虞。E’超過500MPa時，有於樹脂層B之表面產生龜裂之虞，層合體之晶圓之背面研削性變差。又，拉伸斷裂強度未達5MPa時，於晶圓之背面研削時有產生晶圓之剝離之虞。拉伸斷裂強度超過50MPa時，剛性高，產生多數缺陷，無法得到接著特性。　　[0071] E’較佳為5~300MPa、更佳為5~100MPa、又更佳為10~80MPa。樹脂層B之拉伸斷裂強度較佳為10~50MPa。若使用如此之晶圓加工用臨時接著材，則於晶圓之背面研削時，更不易產生晶圓之剝離或晶圓破裂，可更穩定地加工晶圓。　　[0072] 本發明中，儲存模數E’，可使用公知之動態黏彈性測定裝置來測定，拉伸斷裂強度，可使用公知之拉伸試驗機來測定。　　[0073] 樹脂層B，為含有不具有矽氧烷骨架之熱可塑性樹脂(非聚矽氧系熱可塑性樹脂)者。由對具有階差之矽晶圓等的應用性而言，具有良好旋轉塗佈性之非聚矽氧系熱可塑性樹脂特別適宜使用作為形成熱可塑性樹脂層之材料。如此之非聚矽氧系熱可塑性樹脂，特佳為玻璃轉移溫度-80~120℃左右之非聚矽氧系熱可塑性樹脂，Mw較佳為20,000~200,000、更佳可為30,000~150,000者。再者，本發明中，Tg可使用公知之動態黏彈性測定裝置來測定。　　[0074] 前述非聚矽氧系熱可塑性樹脂，可列舉聚烯烴系熱可塑性彈性體、聚丁二烯系熱可塑性彈性體、聚苯乙烯系熱可塑性彈性體、聚苯乙烯/丁二烯系熱可塑性彈性體、聚苯乙烯/烯烴系熱可塑性彈性體等之非聚矽氧系熱可塑性彈性體，特別以耐熱性優良之氫化聚苯乙烯系彈性體為適宜。具體而言可列舉Tuftec(註冊商標)(旭化成Chemicals(股)製)、Espolex(註冊商標)SB系列(住友化學(股)製)、Rabalon(註冊商標)(三菱化學(股)製)、Septon(註冊商標)((股)Kuraray製)、DYNARON(註冊商標)(JSR(股)製)等。又，前述非聚矽氧系熱可塑性樹脂，可列舉以Zeonex(註冊商標)(日本Zeon(股)製)為代表之環烯烴聚合物、以TOPAS(註冊商標)(Topas Advanced Polymers公司製)為代表之環狀烯烴共聚物等。　　[0075] 非聚矽氧系熱可塑性樹脂，較佳為非聚矽氧系熱可塑性彈性體。若為具備含有非聚矽氧系熱可塑性彈性體之層的複合臨時接著劑層，則薄型晶圓製作後，可將該晶圓由支持體容易地剝離，因此可更容易地操作容易破裂之薄型晶圓。　　[0076] 樹脂層B，較佳為由含有前述非聚矽氧系熱可塑性樹脂之樹脂組成物B的硬化物所構成者。　　[0077] 樹脂組成物B，以提高其耐熱性為目的，亦可含有抗氧化劑，或為了提高塗覆性，亦可含有界面活性劑。抗氧化劑可列舉二-tert-丁基酚等。界面活性劑可列舉氟聚矽氧系界面活性劑X-70-1102(信越化學工業(股)製)等。　　[0078] 樹脂組成物B亦可含有溶劑。前述溶劑可列舉烴系溶劑，較佳為壬烷、p-薄荷烷、蒎烯、異辛烷、甲苯、二甲苯、均三甲苯等，由於其塗覆性，更佳為壬烷、p-薄荷烷、異辛烷、均三甲苯。溶劑可1種單獨或混合2種以上使用。前述溶劑之摻合量，相對於樹脂B 100質量份而言，較佳為250~3,500質量份、更佳為300~2,000質量份。　　[0079] 又，樹脂組成物B，亦可使用作為不含溶劑之薄膜狀組成物。　　[0080] 樹脂組成物B為溶液時，可藉由以旋轉塗佈、輥塗佈、模具塗佈、印刷、浸漬等之方法塗佈於晶圓上，之後，以加熱板或烘箱加熱，來形成樹脂層B。此時，加熱條件，通常為於100~200℃、1~10分鐘，較適宜者為於130~190℃、2~5分鐘。　　[0081] 另一方面，樹脂組成物B為薄膜狀組成物時，可藉由層合法於晶圓上形成樹脂層B。　　[0082] 樹脂層B之膜厚，較佳為1~70μm、更佳為2~50μm。膜厚若為前述範圍，則無加熱不足致殘存溶劑之顧慮，且接合時可均勻地覆蓋晶圓上之階差。　　[0083] [晶圓層合體之製造方法] 　　本發明之晶圓層合體之製造方法，包含下述步驟(a)~(e)。 [步驟(a)或(a’)] 　　步驟(a)為於支持體形成具有遮光性之樹脂層A的步驟，步驟(a’)為於支持體形成樹脂組成物層A’之步驟。用以形成樹脂層A之樹脂組成物A為溶液時，藉由將其以旋轉塗佈、輥塗佈等之方法塗佈於支持體上，依其溶劑之揮發條件，較佳為於80~200℃、更佳為於100~180℃之溫度進行預烘烤，使溶劑揮發，藉以形成樹脂組成物層A’。又，樹脂組成物A為薄膜狀組成物時，係藉由層合法於支持體上形成樹脂組成物層A’。　　[0084] 於支持體上所形成之樹脂組成物層A’，係藉由加熱硬化，可作為樹脂層A而發揮功能。加熱硬化可藉由加熱板或烘箱來進行，其溫度通常係100~350℃、較適宜者為150~300℃。又，硬化時間通常係1~10分鐘、較適宜者為2~8分鐘。亦可藉由不使樹脂組成物層A’硬化，形成未硬化狀態之晶圓層合體後，將層合體全體加熱來達成該硬化反應。　　[0085] [步驟(b)或(b’)] 　　步驟(b)為於晶圓之電路形成面形成樹脂層B之步驟，步驟(b’)為於前述樹脂層A或樹脂組成物層A’之上形成樹脂層B之步驟。樹脂組成物B為溶液時，可藉由以旋轉塗佈、輥塗佈、模具塗佈、印刷、浸漬等之方法塗佈於晶圓上，之後，以加熱板或烘箱於130~190℃加熱，來形成樹脂層B。　　[0086] 另一方面，樹脂組成物B為薄膜狀組成物時，可藉由層合法於晶圓上形成樹脂層B。　　[0087] [步驟(c)或(c’)] 　　步驟(c)為將樹脂層A或樹脂組成物A’與樹脂層B於減壓下接合之步驟，步驟(c’)為將前述支持體上之樹脂層B與晶圓之電路形成面於減壓下接合之步驟。減壓條件較佳為0.1~100Pa、更佳為1~80Pa。又，此時，較佳為於40~240℃、更佳為於60~220℃之溫度區域，減壓下將該基板均勻壓接，使其接合即可。　　[0088] [步驟(d)] 　　步驟(d)為進行於步驟(c)或(c’)中接合後之晶圓層合體的樹脂組成物層A’之熱硬化，形成樹脂層A，並且進行與樹脂層B之接合的步驟。前述晶圓層合體形成後，藉由於120~260℃、較佳為150~250℃加熱1分鐘~4小時、較佳為3分鐘~2小時，來進行熱硬化。　　[0089] 如以上所述，可藉由組合支持體、接著劑層及表面具有電路之基板，來得到晶圓層合體。　　[0090] [薄型晶圓之製造方法] 　　藉由將以前述方法所得之晶圓層合體的晶圓之電路非形成面予以研削，可製造薄型晶圓。　　[0091] 接著，藉由對經背面研削而薄型化之晶圓層合體的電路非形成面施以加工，可製造薄型晶圓層合體。該步驟中，包含於晶圓等級所用之各種製程。可列舉電極形成、金屬配線形成、保護膜形成等為例。更具體而言可列舉用於電極等之形成的金屬濺鍍、蝕刻金屬濺鍍層之濕蝕刻、用於作成金屬配線形成之遮罩的阻劑塗佈、曝光，及以顯影形成圖型、阻劑之剝離、乾蝕刻、金屬鍍層之形成、用於TSV形成之矽蝕刻、矽表面之氧化膜形成等以往公知的製程。　　[0092] 薄型晶圓層合體，例如藉由照射355nm之雷射，可自晶圓層合體剝離。 [實施例] 　　[0093] 以下，顯示配製例、實施例及比較例以更具體說明本發明，但本發明不限定於此等實施例。再者，下述例中，份表示質量份。重量平均分子量(Mw)，為使用THF作為溶劑之GPC所得到的聚苯乙烯換算測定值。又，下述例中使用之酸產生劑AG為如以下所示。

[0094] [1]樹脂組成物之配製 [配製例1] 　　於1,000mL之燒瓶中，添加1,5-二羥基萘80g(0.50莫耳)、2-羥基-6-萘醛51.6g(0.30莫耳)及甲基賽珞蘇145g，一邊於70℃攪拌，一邊添加20質量%對甲苯磺酸甲基賽珞蘇溶液20g。將溫度上昇至85℃，攪拌6小時後，冷卻至室溫，以乙酸乙酯800mL稀釋。移至分液漏斗，以去離子水200mL重複洗淨，去除反應觸媒與金屬雜質。將所得之溶液減壓濃縮後，對殘渣添加乙酸乙酯600mL，以己烷2,400mL使聚合物沈澱。將沈澱之聚合物濾離、回收後，減壓乾燥，得到含有下述式表示之重複單位之樹脂A1。樹脂A1之Mw為3,200、分散度(Mw/Mn)為2.44。　　將樹脂A1 20份、酸產生劑AG 1份，及作為交聯劑之Nikalac Mw390((股)三和化學品製)4份，溶解於含有FC-4430(3M公司製)0.1質量%之PGMEA 100份中，以0.1μm之氟樹脂製之濾器過濾，藉以得到樹脂組成物A1。　　又，亦同樣地配製將樹脂溶液A1之PGMEA量變更為35份之組成物，以0.1μm之氟樹脂製之濾器過濾，藉以得到樹脂組成物A1’。

[0095] [配製例2] 　　於1,000mL之燒瓶中，添加1,5-二羥基萘80g(0.50莫耳)、多聚甲醛9.0g(0.30莫耳)及甲基賽珞蘇145g，一邊於70℃攪拌，一邊添加20質量%對甲苯磺酸甲基賽珞蘇溶液20g。將溫度上昇至85℃，攪拌6小時後，冷卻至室溫，以乙酸乙酯800mL稀釋。移至分液漏斗，以去離子水200mL重複洗淨，去除反應觸媒與金屬雜質。將所得之溶液減壓濃縮後，對殘渣添加乙酸乙酯600mL，以己烷2,400mL使聚合物沈澱。將沈澱之聚合物濾離、回收後，減壓乾燥，得到含有下述式表示之重複單位之樹脂A2。樹脂A2之Mw為1,500、Mw/Mn為2.20。　　將樹脂A2 20份、酸產生劑AG 1份，及作為交聯劑之Nikalac Mw390((股)三和化學品製)4份，溶解於含有FC-4430(3M公司製)0.1質量%之PGMEA 100份中，以0.1μm之氟樹脂製之濾器過濾，藉以得到樹脂組成物A2。

[0096] [配製例3] 　　於1,000mL之燒瓶中，添加1-羥基萘72g(0.50莫耳)、2-羥基-6-萘醛51.6g(0.30莫耳)及甲基賽珞蘇145g，一邊於70℃攪拌，一邊添加20質量%對甲苯磺酸甲基賽珞蘇溶液20g。將溫度上昇至85℃，攪拌6小時後，冷卻至室溫，以乙酸乙酯800mL稀釋。移至分液漏斗，以去離子水200mL重複洗淨，去除反應觸媒與金屬雜質。將所得之溶液減壓濃縮後，對殘渣添加乙酸乙酯600mL，以己烷2,400mL使聚合物沈澱。將沈澱之聚合物濾離、回收後，減壓乾燥，得到含有下述式表示之重複單位之樹脂A3。樹脂A3之Mw為2,700、Mw/Mn為2.61。　　將樹脂A3 20份、酸產生劑AG 1份，及作為交聯劑之Nikalac Mw390((股)三和化學品製)4份，溶解於含有FC-4430(3M公司製)0.1質量%之PGMEA 100份中，以0.1μm之氟樹脂製之濾器過濾，藉以得到樹脂組成物A3。

[0097] [比較配製例1] 　　於1,000mL之燒瓶中，添加2-甲基羥基苯32.4g(0.30莫耳)、2-羥基-6-萘醛51.6g(0.30莫耳)及甲基賽珞蘇145g，一邊於70℃攪拌，一邊添加20質量%對甲苯磺酸甲基賽珞蘇溶液20g。將溫度上昇至85℃，攪拌6小時後，冷卻至室溫，以乙酸乙酯800mL稀釋。移至分液漏斗，以去離子水200mL重複洗淨，去除反應觸媒與金屬雜質。將所得之溶液減壓濃縮後，對殘渣添加乙酸乙酯600mL，以己烷2,400mL使聚合物沈澱。將沈澱之聚合物濾離、回收後，減壓乾燥，得到含有下述式表示之重複單位之樹脂A4。樹脂A4之Mw為2,100、Mw/Mn為1.58。　　將樹脂A4 20份、酸產生劑AG 1份，及作為交聯劑之Nikalac Mw390((股)三和化學品製)4份，溶解於含有FC-4430(3M公司製)0.1質量%之PGMEA 100份中，以0.1μm之氟樹脂製之濾器過濾，藉以得到樹脂組成物A4。

[0098] [配製例4] 　　將氫化聚苯乙烯系熱可塑性樹脂Septon 4033((股) Kuraray製聚苯乙烯-聚(乙烯/丙烯)嵌段-聚苯乙烯共聚物，苯乙烯含量30質量%)25g及氫化聚苯乙烯系熱可塑性樹脂Septon 8076((股)Kuraray製聚苯乙烯-聚(乙烯/丁烯)嵌段-聚苯乙烯共聚物，苯乙烯含量30質量%)25g溶解於均三甲苯150g，得到25質量%之Septon 4033/8076之均三甲苯溶液。將所得之溶液以0.2μm之膜濾器過濾，得到樹脂組成物B1。又，測定樹脂之玻璃轉移溫度(Tg)後，係111℃。　　[0099] [配製例5] 　　將氫化聚苯乙烯系熱可塑性樹脂Septon 4033((股) Kuraray製聚苯乙烯-聚(乙烯/丙烯)嵌段-聚苯乙烯共聚物，苯乙烯含量30質量%)25g及氫化聚苯乙烯系熱可塑性樹脂Septon 2002((股)Kuraray製聚苯乙烯-聚(乙烯/丙烯)嵌段-聚苯乙烯共聚物，苯乙烯含量30質量%)25g溶解於均三甲苯150g，得到25質量%之Septon 4033/2002之均三甲苯溶液。將所得之溶液以0.2μm之膜濾器過濾，得到樹脂組成物B2。又，測定樹脂之Tg後，係96℃。　　[0100] [配製例6] 　　將氫化聚苯乙烯系熱可塑性樹脂Septon 4033((股) Kuraray製聚苯乙烯-聚(乙烯/丙烯)嵌段-聚苯乙烯共聚物，苯乙烯含量30質量%)20g及氫化聚苯乙烯系熱可塑性樹脂Tuftec H1051(旭化成((股))製聚苯乙烯-聚(乙烯/丁烯)嵌段-聚苯乙烯共聚物，苯乙烯含量42質量%)20g溶解於均三甲苯160g，得到20質量%之Septon 4033/Tuftec H1051之均三甲苯溶液。將所得之溶液以0.2μm之膜濾器過濾，得到樹脂組成物B3。又，測定樹脂之Tg後，係101℃。　　[0101] [比較配製例2] 　　將氫化聚苯乙烯系熱可塑性樹脂Tuftec H1043(旭化成((股))製聚苯乙烯-聚(乙烯/丁烯)嵌段-聚苯乙烯共聚物，苯乙烯含量67質量%)10g溶解於均三甲苯190g，得到5質量%之Tuftec H1043之均三甲苯溶液。將所得之溶液以0.2μm之膜濾器過濾，得到樹脂組成物B4。又，測定樹脂之Tg後，係107℃。　　[0102] 再者，樹脂之Tg之測定方法係如以下所述。 [Tg之測定方法] 　　將樹脂組成物B1~B4於180℃加熱10分鐘使其硬化，製作厚度0.5mm、30mm×10mm方形之測定薄片。使用所製作之測定薄片，藉由動態黏彈性測定裝置((股)日立High-Tech Science製DMA7100)，以頻率1Hz、昇溫速度3℃/分之條件，於0~300℃之範圍進行測定，以tanδ之波峰(極大值)為Tg。　　[0103] [2]晶圓層合體之製作及其評估 [實施例1~6、比較例1~3] 　　於直徑200mm(厚度：500μm)之玻璃板，旋轉塗佈樹脂組成物A1、A1’、A2、A3或A4後，於加熱板於180℃加熱2分鐘、於250℃加熱5分鐘，藉以使對應於樹脂層A之材料以表1所示之膜厚成膜。　　進一步地，於在表面整面形成有高10μm、直徑40μm之銅柱的直徑200mm矽晶圓(厚度：725μm)之銅柱面，或樹脂層A上，旋轉塗佈均三甲苯溶液B1、B2、B3或B4後，藉由加熱板於150℃加熱5分鐘、於180℃加熱5分鐘，藉此以表1所示之膜厚形成熱可塑性樹脂層B。　　以玻璃板-樹脂層A與樹脂層B-晶圓，或玻璃板-樹脂層A-樹脂層B與晶圓之組合，以樹脂面彼此或樹脂層B與晶圓之銅柱面對合的方式，於真空貼合裝置(EVG公司製、EVG520IS)內，在1Pa以下之減壓條件下，以表1所示之條件貼合，製作晶圓層合體。　　之後，對該接合後之基板進行下述試驗。結果示於表1。再者，由以下之順序實施評估。　　[0104] (1)接著性試驗　　200mm之晶圓接合，係使用EVG公司之晶圓接合裝置EVG520IS進行。接合溫度以表1記載之值、接合時之腔室內壓力以1Pa以下、荷重以20kN來實施。接合後，冷卻至室溫，以目視及光學顯微鏡分別確認其後之界面接合狀況，將未產生於界面之氣泡等之異常的情況評估為良好以「○」表示，將產生異常的情況評估為不良以「×」表示。　　[0105] (2)背面研削耐性試驗　　以研磨機((股)DISCO製、DAG810)，使用金剛石磨石進行矽晶圓之背面研削。研磨至最終基板厚50μm後，以光學顯微鏡(100倍)調查有無龜裂、剝離等之異常。將未產生異常的情況評估為良好以「○」表示，將產生異常的情況評估為不良以「×」表示。　　[0106] (3)CVD耐性試驗　　將背面研削矽晶圓後之層合體導入於CVD裝置，進行2μm之SiO₂ 膜的生成實驗，調查此時有無外觀異常。將未產生外觀異常的情況評估為良好以「○」表示，將產生孔隙、晶圓隆起、晶圓破損等之外觀異常的情況評估為不良以「×」表示。CVD耐性試驗之條件係如以下所述。　　裝置名：電漿CVD PD270STL(Samco(股)製) 　　RF500W、內壓40Pa 　　TEOS(正矽酸四乙酯)：O₂ =20sccm：680sccm 　　[0107] (4)支持體剝離性試驗　　支持體之剝離性係由以下之方法評估。首先，使用切割框於結束CVD耐性試驗之晶圓層合體之薄型化至50μm的晶圓側貼上切割膠帶，將該切割膠帶面藉由真空吸附設置於吸附板。之後，自支持體側對整面照射355nm之雷射。將可將支持體及50μm晶圓不破裂地剝離的情況以「○」表示，將產生破裂等之異常的情況評估為不良以「×」表示。　　[0108] (5)洗淨去除性試驗　　前述剝離性試驗結束後，由以下方法來評估溶劑之洗淨去除性的試驗。將透過切割膠帶安裝於切割框的200mm晶圓(經暴露於CVD耐性試驗條件者)，樹脂層B朝上設置於旋轉塗佈器，使用p-薄荷烷作為洗淨溶劑，進行5分鐘噴霧作為洗淨方法，一邊將晶圓旋轉一邊將異丙醇(IPA)以噴霧進行潤洗。之後，觀察外觀，目視確認有無殘存之樹脂層B。以未觀察到樹脂殘存者評估為良好以「○」表示，以觀察到樹脂殘存者為不良以「×」表示。　　[0109] (6)透過性試驗　　將樹脂組成物A1、A1’、A2、A3或A4，於厚度500μm之玻璃基板旋轉塗佈為膜厚0.3μm後，於250℃進行5分鐘熱硬化，形成樹脂層A，使用分光光度計(U-4100型、(股)日立High-Tech Science製)測定其透過率(波長355nm)。以透過率20%以下之情況為良好以「○」表示，以高於20%的情況為不良以「×」表示。　　[0110] 再者，測定使用樹脂溶液A1、A1’、A2、A3於支持基板上所形成的樹脂層A之透過率後，確認到吸收極大波長均為300~500nm。　　[0111] (7)儲存模數之測定　　將樹脂組成物B1~B4於180℃加熱10分鐘使其硬化，製作厚度0.5mm、30mm×10mm方形之測定薄片。使用所製作之測定薄片，藉由動態黏彈性測定裝置((股)日立High-Tech Science製DMA7100)，以頻率1Hz、昇溫速度3℃/分之條件，於0~300℃之範圍進行測定，以於25℃之值為儲存模數。　　[0112] (8)拉伸斷裂強度之測定　　將樹脂組成物B1~B4於180℃加熱10分鐘使其硬化，由厚度0.4mm、200mm×40mm方形之薄片製作五號啞鈴片。使用所製作之測定薄片，藉由拉伸試驗機((股)東洋精機製作所製V10D)，以拉伸速度50mm/分之條件進行測定，以測定薄片斷裂時的強度為斷裂強度(MPa)。　　[0113]

[0114] 如表1所示，可知實施例1~6中，臨時接著及剝離為容易。另一方面，比較例1中，雷射照射後，支持體未剝離，產生破裂，比較例2中，確認到接合後孔隙，比較例3中，於樹脂層B之塗佈後產生龜裂。再者，實施例1~6中，藉由SEM-EDX試驗測定洗淨後之晶圓表面後，確認到金屬污染(金屬：Ca、K、Na、Mg、Mn、Pb)均為成為問題之等級以下。　　[0115] 再者，本發明不限定於前述實施形態。前述實施形態係為例示，具有與本發明之申請專利範圍所記載之技術思想實質上相同之構成，發揮同樣之作用效果者，均包含於本發明之技術範圍中。[0013] The wafer laminate of the present invention is a wafer that has a support, an adhesive layer formed on the support, and a wafer laminated on the adhesive layer with a circuit surface facing the surface Wafer laminate. The adhesive layer is composed of a resin layer A having light-shielding properties and a resin layer B containing a non-silicone thermoplastic resin in this order from the support side. [0014] The structure of the wafer laminate of the present invention is specifically described. For example, as shown in FIG. 1, a support 1 and a wafer 3 are joined by an adhesive layer 2. The adhesive layer 2 is composed of two layers of a resin layer 2a formed adjacent to the support 1 and a resin layer 2b formed adjacent to the resin layer 2a. [0015] [Support] The aforementioned support includes a transparent substrate, a silicon wafer, a ceramic substrate, etc., and from the viewpoint of the permeability of the laser irradiated when the support is peeled off, a transparent substrate is preferred. For the aforementioned transparent substrate, a glass substrate or a quartz substrate can generally be used, and its thickness is generally preferably 300 to 1,000 μm, more preferably 500 to 800 μm. [0016] [Wafer] The aforementioned wafer is usually a semiconductor wafer. Examples of the semiconductor wafer include silicon wafers, germanium wafers, gallium-arsenic wafers, gallium-phosphorus wafers, gallium-arsenic-aluminum wafers, and the like. The thickness of the aforementioned wafer is not particularly limited, and is usually preferably 600-800 μm, more preferably 625-775 μm. [Resin layer A] The resin layer A is a resin containing a condensed ring in the main chain. It is a resin layer (light-shielding layer) with light-shielding properties. The transmittance of light with a wavelength of 355nm is preferably 20% or less, It is more preferably 18% or less, and still more preferably 15% or less. In addition, the maximum absorption wavelength of the resin layer A is preferably 300 to 500 nm, more preferably 300 to 400 nm. Furthermore, the resin layer A preferably has a transmittance of light with a wavelength of 300 to 500 nm of 20% or less. [0018] From the viewpoints of heat resistance, adhesiveness, chemical resistance, etc., the resin contained in the resin layer A is preferably composed of a cured product of the resin composition A, and the resin composition A contains Resin A is a repeating unit represented by the following formula (1). The repeating unit represented by formula (1) may contain only one type or two or more types.

[0019] In the formula (1), R ¹ to R ³ are each independently a hydrogen atom, a hydroxyl group, or a monovalent organic group having 1 to 20 carbons, preferably 1 to 10. However, ^{at least one of R 1} to R ³ is a hydroxyl group. [0020] The aforementioned monovalent organic group includes methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, tert-butyl, n-pentyl, neopentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-dodecyl, n-pentadecyl, n-eicosyl, cyclopentyl, cyclo Hexyl, cyclopentyl methyl, cyclohexyl methyl, cyclopentyl ethyl, cyclohexyl ethyl, cyclopentyl butyl, cyclohexyl butyl, adamantyl, etc. linear, branched or cyclic Alkyl groups with 1 to 20 carbons; linear, branched or cyclic alkoxy groups with 1 to 5 carbons such as methoxy; epoxy-containing groups such as glycidoxy; phenyl , Naphthyl and other aryl groups. R ¹ to R ^{3 are} preferably hydrogen atoms, hydroxyl groups, methyl groups, and the like. [0021] In the formula (1), R ⁴ is a hydrogen atom, or a monovalent organic group having 1 to 30 carbon atoms, preferably 1 to 10 carbon atoms, which may have a substituent. The ^{monovalent organic group represented by R 4} includes an alkyl group, a phenyl group, a naphthyl group, an anthryl group, a norbornyl group, etc. A part of these hydrogen atoms may also be substituted by an alkyl group, an aryl group, an aldehyde group, and a halogen atom. , Nitro, nitrile, hydroxyl and other substitutions. [0022] Resin A can usually be obtained by polycondensation reaction of naphthol or its derivatives with aldehyde compounds at room temperature or under cooling or heating as needed in solvent-free or solvent-free acid or alkali. get. [0023] The aforementioned naphthol or its derivatives include 1-naphthol, 2-naphthol, 2-methyl-1-naphthol, 4-methoxy-1-naphthol, and 7-methoxy- 2-naphthol, 1,2-dihydroxynaphthalene, 1,3-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 1,4-dihydroxynaphthalene, 1,5-dihydroxynaphthalene, 1,6-dihydroxynaphthalene Hydroxynaphthalene, 2,6-dihydroxynaphthalene, 1,7-dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 1,8-dihydroxynaphthalene, 5-amino-1-naphthol, 2-methoxy Carbonyl-1-naphthol, 1-(4-hydroxyphenyl)naphthalene, 6-(4-hydroxyphenyl)-2-naphthol, 6-(cyclohexyl)-2-naphthol, 1,1'- Bi-2-naphthol, 6,6'-bi-2-naphthol, 9,9-bis(6-hydroxy-2-naphthyl) stilbene, 6-hydroxy-2-vinylnaphthalene, 1-hydroxymethyl Base naphthalene, 2-hydroxymethyl naphthalene, etc. The aforementioned naphthol or its derivatives can be used singly or in combination of two or more kinds. [0024] The aforementioned aldehyde compound may be represented by the following formula (2). R ⁴ -CHO (2) (wherein R ⁴ is the same as described above). [0025] The aldehyde compound represented by the formula (2) includes, for example, formaldehyde, trioxane, paraformaldehyde, acetaldehyde, propionaldehyde, adamantane formaldehyde, benzaldehyde, phenylacetaldehyde, α-phenylpropanal, β-phenylpropionaldehyde, o-chlorobenzaldehyde, m-chlorobenzaldehyde, p-chlorobenzaldehyde, o-nitrobenzaldehyde, m-nitrobenzaldehyde, p-nitrobenzaldehyde, o-methyl Benzaldehyde, m-methylbenzaldehyde, p-methylbenzaldehyde, p-ethylbenzaldehyde, pn-butylbenzaldehyde, 1-naphthaldehyde, 2-naphthaldehyde, anthracenealdehyde, pyrene formaldehyde, furfural, two Methylal, o-phthalaldehyde, isophthalaldehyde, terephthalaldehyde, naphthalene dialdehyde, anthracene dialdehyde, pyrene dialdehyde, etc. The aforementioned aldehyde compounds can be used singly or in combination of two or more kinds. [0026] The solvent used in the aforementioned polycondensation reaction includes, for example, methanol, ethanol, isopropanol, butanol, ethylene glycol, propylene glycol, diethylene glycol, glycerin, methyl serosol, ethyl serosol, Alcohols such as butyl serosol and propylene glycol monomethyl ether; diethyl ether, dibutyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether, tetrahydrofuran (THF), 1 ,4-dioxane and other ethers; dichloromethane, chloroform, dichloroethane, trichloroethylene and other chlorine-based solvents; hexane, heptane, benzene, toluene, xylene, cumene and other hydrocarbons Classes; Nitriles such as acetonitrile; Ketones such as acetone, ethyl methyl ketone, isobutyl methyl ketone; Esters such as ethyl acetate, n-butyl acetate, propylene glycol methyl ether acetate, etc.; γ-butyl Lactones such as lactones; aprotic polar solvents such as dimethyl sulfide, N,N-dimethylformamide, and hexamethylphosphotriamide. These solvents can be used singly or as a mixture of two or more. These solvents are preferably used in the range of 0 to 2,000 parts by mass, and more preferably in the range of 10 to 2,000 parts by mass relative to the total of 100 parts by mass of naphthol or its derivatives and aldehyde compounds. [0027] The acid catalyst used in the aforementioned polycondensation reaction includes, for example, inorganic acids such as hydrochloric acid, hydrobromide acid, sulfuric acid, nitric acid, phosphoric acid, and heteropoly acid; oxalic acid, trifluoroacetic acid, methanesulfonic acid, benzenesulfonic acid, etc. , P-toluenesulfonic acid, trifluoromethanesulfonic acid and other organic acids; aluminum trichloride, ethoxylate, aluminum isopropoxide, boron trifluoride, boron trichloride, boron tribromide, tin tetrachloride , Tin tetrabromide, dibutyltin dichloride, dibutyltin dimethoxide, dibutyltin oxide, titanium tetrachloride, titanium tetrabromide, titanium methoxide (IV), titanium ethoxide (IV), titanium isopropoxide (IV), Titanium (IV) and other road free acids. [0028] In addition, the alkali catalyst used in the aforementioned polycondensation reaction includes, for example, sodium hydroxide, potassium hydroxide, barium hydroxide, sodium carbonate, sodium bicarbonate, potassium carbonate, lithium hydride, sodium hydride, potassium hydride, and hydrogenation. Inorganic bases such as calcium; metal alkyls such as methyl lithium, n-butyl lithium, methyl magnesium chloride, ethyl magnesium bromide, etc.; sodium methoxide, sodium ethoxide, tert-potassium butoxide, etc. Alkoxides; organic bases such as triethylamine, diisopropylethylamine, N,N-dimethylaniline, pyridine, 4-dimethylaminopyridine, etc. [0029] The usage amount of the catalyst is preferably in the range of 0.001 to 100 parts by mass, more preferably in the range of 0.005 to 50 parts by mass relative to the total of 100 parts by mass of naphthol or its derivatives and aldehyde compounds. The reaction temperature is preferably from -50°C to about the boiling point of the solvent, more preferably from room temperature to 100°C. [0030] The polycondensation reaction method includes a method of feeding naphthol or its derivatives, aldehydes, and catalysts at once, or a method of dropping naphthol or its derivatives, or aldehydes in the presence of a catalyst. [0031] The use ratio of naphthol or its derivatives to aldehyde compound, relative to the total naphthol or its derivatives, the aldehyde compound is in molar ratio, preferably 0.01 to 5, more preferably 0.05 to 2 , More preferably 0.05~1, most preferably 0.1~0.9. [0032] After the polycondensation reaction is completed, in order to remove the unreacted raw materials, catalysts, etc. present in the system, the temperature of the reactor can be increased to 130~230°C, and the volatile components can be removed at about 1~50mmHg, or appropriate Different solvents or water to distinguish the polymer, or dissolve the polymer in a good solvent and re-precipitate in a poor solvent. These can be used separately according to the properties of the obtained reaction product. [0033] The weight average molecular weight (Mw) of the resin A is preferably 500 to 500,000, more preferably 1,000 to 100,000. The dispersion degree of the aforementioned polymer is preferably in the range of 1.2-20. If the monomer component, oligomer component, or low molecular weight body with Mw less than 500 is removed, the volatile components during baking can be suppressed, and baking can be prevented. Surface defects caused by pollution around the baking cup or falling of volatile components. In addition, in the present invention, Mw refers to a polystyrene conversion value obtained by gel permeation chromatography (GPC) using THF as a solvent. [0034] The resin composition A preferably contains a crosslinking agent that crosslinks the resin A by thermal reaction. The aforementioned crosslinking agent is suitable to use epoxy compounds having more than two functional groups in the molecule, epoxy resins, amine-based resins such as methylol melamine, etc., in order to promote the crosslinking of these crosslinking agents with the aforementioned polymers For the reaction, it is preferable to further add a catalyst. [0035] The aforementioned epoxy compounds or epoxy resins include bifunctional, trifunctional, and tetrafunctional or more polyfunctional epoxy resins, such as EOCN-1020 (refer to the following formula) manufactured by Nippon Kayaku Co., Ltd., EOCN -102S, XD-1000, NC-2000-L, EPPN-201, GAN, NC6000, or those expressed by the following formula, etc. [0036]

[0037] When the aforementioned epoxy compound or epoxy resin is used as the crosslinking agent, the blending amount is preferably 0.1-50 mass parts relative to 100 parts by mass of the polymer having the repeating unit represented by formula (1) Parts, more preferably 0.1-30 parts by mass, still more preferably 1-30 parts by mass. The crosslinking agent can be used singly or in combination of two or more kinds. If the blending amount is in the aforementioned range, a sufficient crosslinking density can be obtained, and the resulting cured product can fully function. [0038] Furthermore, when the aforementioned epoxy resin is used as a crosslinking agent, it is preferable to add a hardening accelerator as a catalyst. By containing the epoxy resin hardening accelerator, the hardening reaction can proceed appropriately and uniformly. [0039] Epoxy resin hardening accelerators, for example, 2-methylimidazole, 2-ethylimidazole, 2-ethyl-4-methylimidazole, and ethyl isocyanate compounds of these compounds; 2- Phenylimidazole, 2-phenyl-4-methylimidazole, 2-phenyl-4-methyl-5-hydroxymethylimidazole, 2-phenyl-4,5-dihydroxymethylimidazole and other imidazole compounds ; 1,8-diazabicyclo[5.4.0]undecene-7 (DBU), 1,5-diazabicyclo[4.3.0]nonene-5 (DBN), the organic acid salt of DBU, DBU series compounds such as phenol resin salt of DBU, tetraphenyl borate of DBU derivative; triphenylphosphine, tributylphosphine, ginseng (p-methylphenyl) phosphine, ginseng (p-methoxybenzene) Phosphonium) phosphine, ginseng (p-ethoxyphenyl) phosphine, triphenyl phosphine/triphenyl borate, tetraphenyl phosphine/tetraphenyl borate and other three organic phosphines; 4-level phosphonium salt; triethyl Tertiary amines such as ammonium/triphenyl borate, and its tetraphenyl borate, etc. The aforementioned epoxy resin hardening accelerator may be used singly or in combination of two or more kinds. [0040] The blending amount of the epoxy resin hardening accelerator is preferably 0.1-10 parts by mass, more preferably 0.2-5 parts by mass relative to 100 parts by mass of the resin A. [0041] In addition, amino resins such as methylol melamine used in the present invention may be selected from amine condensates modified by formalin or formalin-alcohol and having an average of 2 or more hydroxyl groups per molecule. One or more compounds from the group of methyl or alkoxymethylol phenol compounds. [0042] The aforementioned amino resin preferably has a Mw of 150 to 10,000, and more preferably has a Mw of 200 to 3,000. If Mw is in the aforementioned range, sufficient curability can be obtained, and the heat resistance of the composition after curing is also good. [0043] The aforementioned amine-based condensate modified by formalin or formalin-alcohol, for example, can include melamine condensate modified by formalin or formalin-alcohol, or modified by formalin or formalin-alcohol. Urea condensate. [0044] The aforementioned melamine condensate modified by formalin or formalin-alcohol, for example, can be modified by hydroxymethylation of melamine monomer with formalin according to known methods, or further alkoxylated with alcohol The modified melamine was prepared as modified melamine represented by the following formula. Furthermore, as the aforementioned alcohol, a lower alcohol, for example, an alcohol having 1 to 4 carbon atoms is preferred. [0045]

(In the formula, R ⁵ to R ¹⁰ are each independently a hydroxymethyl group; an alkoxymethyl group containing a linear, branched or cyclic alkoxy group with 1 to 4 carbon atoms; or a hydrogen atom, However, at least one is hydroxymethyl or alkoxymethyl). [0046] The aforementioned modified melamine includes trimethoxymethyl monomethylol melamine, dimethoxymethyl monomethylol melamine, trimethylol melamine, hexamethylol melamine, and hexamethoxymethylol Based on melamine and so on. Then, by adding the modified melamine or the polymers obtained therefrom (for example, dimers, trimers, etc. oligomers) according to the general method, addition condensation polymerization is performed until it becomes formaldehyde and the desired molecular weight. The melamine condensate modified by formalin or formalin-alcohol is obtained. Furthermore, one or more modified melamine condensates of the aforementioned modified melamine and its condensate can be used as a crosslinking agent. [0047] In addition, the urea condensate modified by formalin or formalin-alcohol can be modified by, for example, following a known method by hydroxymethylating a urea condensate with a desired molecular weight with formalin, or It is further formulated with alcohol alkoxylation and modification. [0048] Specific examples of the aforementioned modified urea condensate include, for example, a methoxymethylated urea condensate, an ethoxymethylated urea condensate, and a propoxymethylated urea condensate. Furthermore, one or more of these modified urea condensates can be used. [0049] Among these, as a phenol compound having an average of two or more hydroxymethyl groups or alkoxymethylol groups in one molecule, for example, (2-hydroxy-5-methyl)-1,3- Benzene dimethanol, 2,2',6,6'-tetramethoxymethyl bisphenol A, etc. [0050] These amino condensates or phenol compounds can be used alone or in combination of two or more. [0051] The blending amount of the aforementioned crosslinking agent is preferably 0.1-50 parts by mass, and more preferably 1-30 parts by mass relative to 100 parts by mass of resin A. If it is in the aforementioned range, the composition A will be fully cured, and the resulting cured product will fully function. [0052] Furthermore, when using the aforementioned amino resin such as methylol melamine as a crosslinking agent, it is preferable to add a thermal acid generator as a catalyst. The thermal acid generator is not particularly limited, and examples thereof include ammonium salts represented by the following formula.

(In the formula, R ¹¹ to R ¹⁴ each independently represent a hydrogen atom; linear, branched or cyclic alkyl group with 1 to 12 carbons or pendant oxyalkyl group; linear, branched or Cyclic alkenyl or pendant oxyalkenyl with 2-12 carbons; aryl with 6-20 carbons; or aralkyl or aryl pendant oxyalkyl with 7-12 carbons, among these groups Part or all of the hydrogen atoms may be substituted by alkoxy groups. ^{Two selected from R 11} to R ¹⁴ may also form a ring together with the nitrogen atom to which they are bonded. The ring has a formula in the ring The nitrogen atom has an aliphatic ring with 3 to 10 carbon atoms, or a heteroaromatic ring with 5 to 10 carbon atoms in the ring having the nitrogen atom in the formula. X ^- is a sulfonic acid in which at least one of the α-position is fluorinated, Perfluoroalkylimidic acid or perfluoroalkylmethylated acid). [0053] X ^- Specifically, perfluoroalkanesulfonic acid anions such as trifluoromethanesulfonic acid anion and nonafluorobutanesulfonic acid anion; sulfonic acid anion in which at least one of the α-position is substituted by fluorine; bis(trifluoro Methylsulfonyl) iminium anion, bis (perfluoroethyl sulfonyl) iminium anion, bis (perfluorobutyl sulfonyl) iminium anion, etc.; see (three Fluoromethylsulfonyl) methyl body anion, ginseng (perfluoroethylsulfonyl) methyl body anion, etc. methyl body (methanide) anion. [0054] The blending amount of the thermal acid generator is preferably 0.1-15 parts by mass, more preferably 0.2-10 parts by mass, relative to 100 parts by mass of the resin A. If it is in the aforementioned range, the composition A is sufficiently hardened, and the storage stability of the composition A is also good. [0055] The resin composition A may also contain a solvent. Examples of the aforementioned solvent include ketones such as cyclohexanone, cyclopentanone, and methyl-2-n-pentyl ketone; 3-methoxybutanol, 3-methyl-3-methoxybutanol, 1 -Methoxy-2-propanol, 1-ethoxy-2-propanol and other alcohols; propylene glycol monomethyl ether, ethylene glycol monomethyl ether, propylene glycol monoethyl ether, ethylene glycol monoethyl Base ether, propylene glycol dimethyl ether, diethylene glycol dimethyl ether, etc.; propylene glycol monomethyl ether acetate, propylene glycol monoethyl ether acetate, ethyl lactate, ethyl pyruvate, acetic acid Butyl ester, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, tert-butyl acetate, tert-butyl propionate, propylene glycol mono-tert-butyl ether acetate, γ- Butyrolactone and other esters. These can be used singly or as a mixture of two or more. The blending amount of the aforementioned solvent is preferably 100 to 5,000 parts by mass, more preferably 150 to 2,500 parts by mass relative to 100 parts by mass of resin A. [0056] In addition, the resin composition A can also be used as a solvent-free film-like composition. [0057] The resin composition A may contain a surfactant as needed, or may contain an antioxidant or the like for the purpose of further improving heat resistance. [0058] The surfactant is not particularly limited, and examples include polyoxyethylene alkyl such as polyoxyethylene lauryl ether, polyoxyethylene stearyl ether, polyoxyethylene cetyl ether, polyoxyethylene oleyl ether, etc. Ethers; polyoxyethylene alkyl aryl ethers such as polyoxyethylene octyl phenol ether and polyoxyethylene nonyl phenol ether; polyoxyethylene polyoxypropylene block copolymers; sorbitan monolaurate, Sorbitan fatty acid esters such as sorbitan monopalmitate and sorbitan monostearate; polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monopalmitate, polyoxyethylene Nonionic surfactants of polyoxyethylene sorbitan fatty acid esters such as sorbitan monostearate, polyoxyethylene sorbitan trioleate, polyoxyethylene sorbitan tristearate, etc.; Eftop (registered trademark) EF301, EF303, EF352 (manufactured by Tokem Products), Megafac (registered trademark) F171, F172, F173 (DIC (share) system), Fluorad (registered trademark) FC430, FC431 (manufactured by 3M Corporation) , Asahiguard AG710, Surflon (registered trademark) S-381, S-382, SC101, SC102, SC103, SC104, SC105, SC106, Sufynol (registered trademark) E1004, KH-10, KH-20, KH-30, KH- 40 (Asahi Glass Co., Ltd.) and other fluorine-based surfactants; organosiloxane polymer KP341, X-70-092, X-70-093, X-70-1102 (manufactured by Shin-Etsu Chemical Co., Ltd.), Acrylic or methacrylic POLYFLOW No. 75, No. 95 (manufactured by Kyoeisha Chemical Co., Ltd.). These can be used individually by 1 type or in combination of 2 or more types. [0059] The antioxidant is preferably at least one selected from hindered phenol-based compounds, hindered amine-based compounds, organophosphorus compounds, and organosulfur compounds. [0060] The aforementioned hindered phenol-based compound is not particularly limited, but is preferably the one listed below. For example, 1,3,5-trimethyl-2,4,6-ginseng (3,5-di-tert-butyl-4-hydroxybenzyl)benzene (trade name: IRGANOX 1330), 2,6 -Di-tert-butyl-4-methylphenol (trade name: Sumilizer BHT), 2,5-di-tert-butyl-hydroquinone (trade name: Nocrac NS-7), 2,6-di- tert-butyl-4-ethylphenol (trade name: Nocrac M-17), 2,5-di-tert-pentylhydroquinone (trade name: Nocrac DAH), 2,2'-methylene bis( 4-methyl-6-tert-butylphenol) (trade name: Nocrac NS-6), 3,5-di-tert-butyl-4-hydroxy-benzylphosphonate-diethyl ester (commodity Name: IRGANOX 1222), 4,4'-thiobis(3-methyl-6-tert-butylphenol) (trade name: Nocrac 300), 2,2'-methylenebis(4-ethyl- 6-tert-butylphenol) (trade name: Nocrac NS-5), 4,4'-butylene bis(3-methyl-6-tert-butylphenol) (trade name: ADK STAB AO-40) , 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate (trade name: Sumilizer GM), 2-[1 -(2-Hydroxy-3,5-di-tert-pentylphenyl)ethyl]-4,6-di-tert-pentylphenyl acrylate (trade name: Sumilizer GS), 2,2'- Methylenebis[4-methyl-6-(α-methyl-cyclohexyl)phenol], 4,4'-methylenebis(2,6-di-tert-butylphenol) (trade name: Seenox 226M), 4,6-bis(octylthiomethyl)-o-cresol (trade name: IRGANOX 1520L), 2,2'-ethylenebis(4,6-di-tert-butylphenol) , Octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate (trade name: IRGANOX 1076), 1,1,3-shen-(2-methyl -4-Hydroxy-5-tert-butylphenyl)butane (trade name: ADK STAB AO-30), tetrakis[methylene-(3,5-di-tert-butyl-4-hydroxyhydrocinnabar) Ester)] methane (trade name: ADK STAB AO-60), triethylene glycol bis[3-(3-tert-butyl-5-methyl-4-hydroxyphenyl) propionate] (trade name ：IRGANOX 245), 2,4-bis-(n-octylthio)-6-(4-hydroxy-3,5-di-tert-butylanilino)-1,3,5-triazine (commodity Name: IRGANOX 565), N,N'-hexamethylene bis(3,5-di-tert- Butyl-4-hydroxy-hydrocinnamidine) (trade name: IRGANOX 1098), 1,6-hexanediol-bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl) Propionate] (trade name: IRGANOX 259), 2,2-sulfanyl-diethylenebis[3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate] (commodity Name: IRGANOX 1035), 3,9-bis[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionyloxy]1,1-dimethylethyl ]2,4,8,10-Tetraoxaspiro[5.5]undecane (trade name: Sumilizer GA-80), ginseng-(3,5-di-tert-butyl-4-hydroxybenzyl) iso Cyanurate (trade name: IRGANOX 3114), bis(3,5-di-tert-butyl-4-hydroxybenzylphosphonate ethyl ester) calcium/polyethylene wax mixture (50:50) (trade name ：IRGANOX 1425WL), isooctyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate (trade name: IRGANOX 1135), 4,4'-thiobis(6 -tert-butyl-3-methylphenol) (trade name: Sumilizer WX-R), 6-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propoxy] -2,4,8,10-tetra-tert-butyldibenzo[d,f][1,3,2]dioxaphosphapine (trade name: Sumilizer GP) and the like. [0061] The aforementioned hindered amine compound is not particularly limited, but is preferably one listed below. For example, p,p'-dioctyl diphenylamine (trade name: IRGANOX 5057), phenyl-α-naphthylamine (Nocrac PA), poly(2,2,4-trimethyl-1,2-diphenylamine) Hydroquinoline) (trade name: Nocrac 224, 224-S), 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline (trade name: Nocrac AW), N, N'-Diphenyl-p-phenylenediamine (trade name: Nocrac DP), N,N'-bis-β-naphthyl-p-phenylenediamine (trade name: Nocrac White), N-phenyl- N'-isopropyl-p-phenylenediamine (trade name: Nocrac 810NA), N,N'-diallyl-p-phenylenediamine (trade name: Nonflex TP), 4,4'-(α ,α-Dimethylbenzyl)diphenylamine (trade name: Nocrac CD), p,p-toluenesulfonylamino diphenylamine (trade name: Nocrac TD), N-phenyl-N'-(3- Methacryloxy-2-hydroxypropyl)-p-phenylenediamine (trade name: Nocrac G1), N-(1-methylheptyl)-N'-phenyl-p-phenylenediamine ( Trade name: Ozonon 35), N,N'-di-sec-butyl-p-phenylenediamine (trade name: Sumilizer BPA), N-phenyl-N'-1,3-dimethylbutyl- p-phenylenediamine (trade name: Antigene 6C), alkylated diphenylamine (trade name: Sumilizer 9A), succinate dimethyl-1-(2-hydroxyethyl)-4-hydroxy-2,2, 6,6-Tetramethylpiperidine polycondensate (trade name: Tinuvin 622LD), poly[[6-(1,1,3,3-tetramethylbutyl)amino-1,3,5-tri Oxazine-2,4-diyl][(2,2,6,6-tetramethyl-4-piperidinyl)imino]hexamethylene[(2,2,6,6-tetramethyl -4-piperidinyl)imino]] (trade name: CHIMASSORB 944), N,N'-bis(3-aminopropyl)ethylenediamine-2,4-bis[N-butyl-N -(1,2,2,6,6-Pentamethyl-4-piperidinyl)amino]-6-chloro-1,3,5-triazine condensate (trade name: CHIMASSORB 119FL), bis( 1-octyloxy-2,2,6,6-tetramethyl-4-piperidinyl) sebacate (trade name: TINUVIN 123), bis(2,2,6,6-tetramethyl- 4-piperidinyl) sebacate (trade name: TINUVIN 770), 2-(3,5-di-tert-butyl-4-hydroxybenzyl)-2-n-butylmalonic acid bis( 1,2,2,6,6-pentamethyl-4-piperidinyl) (trade name: TINUVIN 144), bis(1,2,2,6,6-pentamethyl-4-piperidinyl) Sebacate (trade name: TINUVIN 76 5), Si (1,2,2,6,6-pentamethyl-4-piperidinyl) 1,2,3,4-butane tetracarboxylic acid ester (trade name: LA-57), Si ( 2,2,6,6-Tetramethyl-4-piperidinyl) 1,2,3,4-butane tetracarboxylate (trade name: LA-52), 1,2,3,4-butane Mixed ester compound of alkanetetracarboxylic acid, 1,2,2,6,6-pentamethyl-4-piperidinol and 1-tridecanol (trade name: LA-62), 1,2,3,4 -Butane tetracarboxylic acid, 2,2,6,6-tetramethyl-4-piperidinol and 1-tridecanol mixed ester (trade name: LA-67), 1,2,3,4 -Butanetetracarboxylic acid and 1,2,2,6,6-pentamethyl-4-piperidinol and 3,9-bis(2-hydroxy-1,1-dimethylethyl)-2, 4,8,10-Tetraoxaspiro[5.5]Undecane mixed ester (trade name: LA-63P), 1,2,3,4-butanetetracarboxylic acid and 2,2,6,6 -Tetramethyl-4-piperidinol and 3,9-bis(2-hydroxy-1,1-dimethylethyl)-2,4,8,10-tetraoxaspiro[5.5]undecane The mixed ester (trade name: LA-68LD), (2,2,6,6-tetramethylene-4-piperidinyl)-2-propylene carboxylate (trade name: ADK STAB LA- 82), (1,2,2,6,6-pentamethyl-4-piperidinyl)-2-propylene carboxylate (trade name: ADK STAB LA-87) and the like. [0062] The aforementioned organophosphorus compound is not particularly limited, but is preferably the one listed below. For example, bis(2,4-di-tert-butylphenyl)[1,1-biphenyl]-4,4'-diyl bisphosphite, 9,10-dihydro-9-oxygen Hetero-10-phosphaphenanthrene-10-oxide (trade name: SANKO-HCA), triethyl phosphite (trade name: JP302), tri-n-butyl phosphite (trade name: JP304), phosphorous acid Triphenyl ester (trade name: ADK STAB TPP), diphenyl monooctyl phosphite (trade name: ADK STAB C), tris(p-cresol) phosphite (trade name: Chelex-PC), Diphenyl monodecyl phosphate (trade name: ADK STAB 135A), diphenyl mono(tridecyl) phosphite (trade name: JPM313), ginseng (2-ethylhexyl) phosphite (trade name) : JP308), phenyl didecyl phosphite (trade name: ADK STAB 517), tridecyl phosphite (trade name: ADK STAB 3010), tetraphenyl dipropylene glycol diphosphite (trade name: JPP100) , Bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite (trade name: ADK STAB PEP-24G), ginseng (tridecyl) phosphite (trade name: JP333E), double (Nonylphenyl) pentaerythritol diphosphite (trade name: ADK STAB PEP-4C), bis(2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite (trade name : ADK STAB PEP-36), bis[2,4-bis(1-phenylisopropyl)phenyl] pentaerythritol diphosphite (trade name: ADK STAB PEP-45), trilauryl trisulfide Phosphate (trade name: JPS312), ginseng (2,4-di-tert-butylphenyl) phosphite (trade name: IRGAFOS 168), ginseng (nonylphenyl) phosphite (trade name: ADK) STAB 1178), distearyl pentaerythritol diphosphite (trade name: ADK STAB PEP-8), ginseng (mono, dinonylphenyl) phosphite (trade name: ADK STAB 329K), three oils of phosphite Esters (trade name: Chelex-OL), tristearyl phosphite (trade name: JP318E), 4,4'-butylene bis(3-methyl-6-tert-butylphenyl di-tridecane Base) phosphite (trade name: JPH1200), tetrakis (C ₁₂ -C ₁₅ mixed alkyl)-4,4'-isopropylidene diphenyl diphosphite (trade name: ADK STAB 1500), tetra (Tridecyl)-4,4'-butylene bis(3-methyl-6-tert-butylphenol) diphosphite (trade name: ADK STAB 260), hexa(tridecyl)- 1,1,3-ginseng (2-methyl-5-tert-butyl-4-hydroxyphenyl) butane-triphosphite (commodity Name: ADK STAB 522A), hydrogenated bisphenol A phosphite polymer (HBP), Si (2,4-di-tert-butylphenoxy) 4,4'-biphenylene-di-phosphine (commodity Name: P-EPQ), Si (2,4-di-tert-butyl-5-methylphenoxy) 4,4'-biphenylene-di-phosphine (trade name: GSY-101P), 2 -[[2,4,8,10-(1,1-Dimethylethyl)dibenzo[d,f][1,3,2]dioxaphosphorin-6-yl] Oxy]-N,N-bis[2-[[2,4,8,10-(1,1-dimethylethyl)dibenzo[d,f][1,3,2]bis Oxaphosphapin-6-yl]oxy]-ethyl]ethylamine (trade name: IRGAFOS 12), 2,2'-methylenebis(4,6-di-tert-butylphenyl) ) Octyl phosphite (trade name: ADK STAB HP-10) and the like. [0063] The aforementioned organosulfur compound is not particularly limited, but is preferably the one listed below. For example, dilauryl-3,3'-thiodipropionate (trade name: Sumilizer TPL-R), dimyristyl-3,3'-thiodipropionate (trade name: Sumilizer TPM), distearyl-3,3'-thiodipropionate (trade name: Sumilizer TPS), pentaerythritol 4 (3-lauryl thiopropionate) (trade name: Sumilizer TP-D), Di-tridecyl-3,3'-thiodipropionate (trade name: Sumilizer TL), 2-mercaptobenzimidazole (trade name: Sumilizer MB), di-tridecyl-3,3 '-Thiodipropionate (trade name: ADK STAB AO-503A), 1,3,5-gin-β-stearylthiopropionyloxyethyl isocyanurate, 3,3 Di-dodecyl'-thiodipropionate (trade name: IRGANOX PS 800FL), 3,3'-thiodipropionate di-octadecyl ester (trade name: IRGANOX PS 802FL) and the like. [0064] Among the aforementioned antioxidants, particularly preferred is tetrakis[methylene-(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)]methane. The amount of the aforementioned antioxidant added is preferably 0.5 to 5 parts by mass, more preferably 1 to 3 parts by mass relative to 100 parts by mass of resin A. If it is the said range, sufficient heat-resistant effect can be acquired, and compatibility can also be acquired. In addition, antioxidants can be used singly or in combination of two or more kinds. [0065] In addition, in order to further improve the heat resistance, in the resin composition A, with respect to 100 parts by mass of the resin A, 50 parts by mass or less of fillers such as well-known silica may be added. [0066] When the resin composition A is a solution, it is coated on the support by spin coating, roll coating, die coating, printing, dipping, etc., depending on the volatilization conditions of the solvent, preferably less than 80 ~200°C, more preferably, pre-baking at a temperature of 100~180°C to volatilize the solvent, thereby forming the resin composition layer A'. [0067] On the other hand, when the resin composition A is a film-like composition, the resin composition layer A'can be formed on the support by a laminating method. [0068] The resin composition layer A'formed on the support is further cured by heating to function as the resin layer A. Heating and hardening can be carried out by a hot plate or an oven. The conditions are usually 100~350℃, 5~10 minutes, preferably 150~300℃, 3~8 minutes. This hardening reaction is achieved by heating the entire laminated body after the wafer laminate body in an uncured state is formed without hardening the resin composition layer A′. [0069] The film thickness of the resin layer A formed on the support is preferably 0.1 to 50 μm, more preferably 0.3 to 30 μm. When the film thickness is in the aforementioned range, the light shielding property is sufficient, and the flatness of the film is also good. [0070] [Resin layer B] The resin layer B has a storage modulus E'of 1 to 500 MPa at 25° C. and a tensile breaking strength of 5 to 50 MPa. When E'is less than 1 MPa, the wafer may peel off during grinding on the back of the resin layer B. When E'exceeds 500 MPa, cracks may occur on the surface of the resin layer B, and the back surface of the laminated wafer may deteriorate. In addition, when the tensile fracture strength is less than 5 MPa, the wafer may peel off during the grinding of the back side of the wafer. When the tensile rupture strength exceeds 50 MPa, the rigidity is high, many defects occur, and adhesive properties cannot be obtained. [0071] E'is preferably 5 to 300 MPa, more preferably 5 to 100 MPa, and still more preferably 10 to 80 MPa. The tensile breaking strength of the resin layer B is preferably 10-50 MPa. If such a temporary bonding material for wafer processing is used, it is less likely to cause wafer peeling or wafer cracking during the backside grinding of the wafer, and the wafer can be processed more stably. [0072] In the present invention, the storage modulus E'can be measured using a known dynamic viscoelasticity measuring device, and the tensile breaking strength can be measured using a known tensile testing machine. [0073] The resin layer B contains a thermoplastic resin (non-silicone-based thermoplastic resin) that does not have a silicone skeleton. In terms of applicability to silicon wafers with a step difference, non-silicone-based thermoplastic resins with good spin coatability are particularly suitable as materials for forming the thermoplastic resin layer. Such a non-silicone thermoplastic resin is particularly preferably a non-silicone thermoplastic resin with a glass transition temperature of -80 to 120°C, and the Mw is preferably 20,000 to 200,000, more preferably 30,000 to 150,000. Furthermore, in the present invention, Tg can be measured using a known dynamic viscoelasticity measuring device. [0074] The aforementioned non-silicone-based thermoplastic resins include polyolefin-based thermoplastic elastomers, polybutadiene-based thermoplastic elastomers, polystyrene-based thermoplastic elastomers, and polystyrene/butadiene-based thermoplastic elastomers. Non-silicone-based thermoplastic elastomers such as thermoplastic elastomers and polystyrene/olefin-based thermoplastic elastomers are particularly suitable for hydrogenated polystyrene-based elastomers with excellent heat resistance. Specifically, Tuftec (registered trademark) (manufactured by Asahi Kasei Chemicals Co., Ltd.), Espolex (registered trademark) SB series (manufactured by Sumitomo Chemical Co., Ltd.), Rabalon (registered trademark) (manufactured by Mitsubishi Chemical Co., Ltd.), Septon (Registered trademark) ((stock) Kuraray system), DYNARON (registered trademark) (JSR (stock) system), etc. In addition, the aforementioned non-polysiloxane-based thermoplastic resins include cycloolefin polymers represented by Zeonex (registered trademark) (manufactured by Zeon Corporation), and TOPAS (registered trademark) (manufactured by Topas Advanced Polymers) as Representative cyclic olefin copolymers, etc. [0075] The non-silicone-based thermoplastic resin is preferably a non-silicone-based thermoplastic elastomer. If it is a composite temporary adhesive layer with a layer containing a non-silicone-based thermoplastic elastomer, after the thin wafer is produced, the wafer can be easily peeled from the support, so it can be handled more easily and easily broken. Thin wafers. [0076] The resin layer B is preferably composed of a cured product of the resin composition B containing the aforementioned non-silicone-based thermoplastic resin. [0077] The resin composition B may contain an antioxidant for the purpose of improving its heat resistance, or may contain a surfactant in order to improve the coatability. Examples of antioxidants include di-tert-butylphenol and the like. Examples of the surfactant include fluoropolysiloxane-based surfactant X-70-1102 (manufactured by Shin-Etsu Chemical Co., Ltd.). [0078] The resin composition B may also contain a solvent. Examples of the aforementioned solvent include hydrocarbon solvents, preferably nonane, p-menthane, pinene, isooctane, toluene, xylene, mesitylene, etc., and more preferably nonane, p-menthane, etc. due to its coatability. Menthane, isooctane, mesitylene. One type of solvent can be used alone or as a mixture of two or more types. The blending amount of the aforementioned solvent is preferably 250 to 3,500 parts by mass, more preferably 300 to 2,000 parts by mass relative to 100 parts by mass of resin B. [0079] In addition, the resin composition B can also be used as a solvent-free film-like composition. [0080] When the resin composition B is a solution, it can be applied to the wafer by spin coating, roll coating, die coating, printing, dipping, etc., and then heated with a hot plate or oven. The resin layer B is formed. At this time, the heating conditions are usually 100 to 200°C for 1 to 10 minutes, preferably 130 to 190°C for 2 to 5 minutes. [0081] On the other hand, when the resin composition B is a film-like composition, the resin layer B can be formed on the wafer by a lamination method. [0082] The film thickness of the resin layer B is preferably 1 to 70 μm, more preferably 2 to 50 μm. If the film thickness is in the aforementioned range, there is no concern about residual solvent due to insufficient heating, and the step difference on the wafer can be uniformly covered during bonding. [0083] [Method for manufacturing a wafer laminate] The method for manufacturing a wafer laminate of the present invention includes the following steps (a) to (e). [Step (a) or (a')] Step (a) is a step of forming a resin layer A having light-shielding properties on the support, and step (a') is a step of forming a resin composition layer A'on the support. When the resin composition A used to form the resin layer A is a solution, it is applied to the support by spin coating, roll coating, etc., depending on the volatilization conditions of the solvent, preferably between 80~ 200°C, more preferably, pre-baking at a temperature of 100 to 180°C to volatilize the solvent, thereby forming the resin composition layer A'. In addition, when the resin composition A is a film-like composition, the resin composition layer A'is formed on the support by a laminating method. [0084] The resin composition layer A'formed on the support is cured by heating to function as the resin layer A. Heating and hardening can be carried out by a hot plate or an oven, and the temperature is usually 100-350°C, preferably 150-300°C. In addition, the curing time is usually 1 to 10 minutes, preferably 2 to 8 minutes. The hardening reaction can also be achieved by heating the entire laminated body without hardening the resin composition layer A′ to form an unhardened wafer laminated body. [Step (b) or (b')] Step (b) is a step of forming a resin layer B on the circuit formation surface of the wafer, and step (b') is on the aforementioned resin layer A or resin composition layer A 'The step of forming a resin layer B above. When the resin composition B is a solution, it can be applied to the wafer by spin coating, roll coating, die coating, printing, dipping, etc., and then heated at 130 to 190°C with a hot plate or oven , To form a resin layer B. [0086] On the other hand, when the resin composition B is a film-like composition, the resin layer B can be formed on the wafer by a lamination method. [Step (c) or (c')] Step (c) is a step of bonding the resin layer A or the resin composition A'and the resin layer B under reduced pressure, and the step (c') is the step of bonding the aforementioned support The step of bonding the resin layer B on the body and the circuit forming surface of the wafer under reduced pressure. The decompression condition is preferably 0.1-100 Pa, more preferably 1-80 Pa. In addition, at this time, it is preferable to uniformly press and bond the substrates in a temperature range of 40 to 240° C., more preferably 60 to 220° C. under reduced pressure to bond them. [Step (d)] Step (d) is to perform thermal curing of the resin composition layer A'of the wafer laminate after bonding in the step (c) or (c') to form the resin layer A, and The step of bonding with the resin layer B is performed. After the aforementioned wafer laminate is formed, it is thermally cured by heating at 120 to 260°C, preferably 150 to 250°C for 1 minute to 4 hours, and preferably 3 minutes to 2 hours. [0089] As described above, a wafer laminate can be obtained by combining a support, an adhesive layer, and a substrate with a circuit on the surface. [0090] [Method for Manufacturing Thin Wafer] By grinding the circuit non-forming surface of the wafer of the wafer laminate obtained by the aforementioned method, a thin wafer can be manufactured. [0091] Next, by processing the circuit non-forming surface of the wafer laminate thinned by back grinding, a thin wafer laminate can be manufactured. This step includes various processes used at the wafer level. Examples include electrode formation, metal wiring formation, protective film formation, and the like. More specifically, metal sputtering used for the formation of electrodes, wet etching for etching metal sputtered layers, resist coating and exposure for forming masks for metal wiring formation, and development of patterns and resists can be mentioned. Conventionally known processes such as the stripping of reagents, dry etching, formation of metal plating, silicon etching for TSV formation, and formation of oxide film on the silicon surface. [0092] The thin wafer laminate can be peeled from the wafer laminate by irradiating a 355nm laser, for example. [Examples] [0093] Hereinafter, preparation examples, examples, and comparative examples are shown to more specifically illustrate the present invention, but the present invention is not limited to these examples. In addition, in the following examples, parts represent parts by mass. The weight average molecular weight (Mw) is a polystyrene conversion measurement value obtained by GPC using THF as a solvent. In addition, the acid generator AG used in the following examples is as shown below.

[1] Preparation of resin composition [Preparation Example 1] In a 1,000 mL flask, 80 g (0.50 mol) of 1,5-dihydroxynaphthalene and 51.6 g (0.30 of 2-hydroxy-6-naphthaldehyde) were added. Mol) and 145 g of methyl serosol, while stirring at 70° C., 20 g of a 20% by mass methyl serosol solution of p-toluenesulfonate was added. The temperature was increased to 85°C, and after stirring for 6 hours, it was cooled to room temperature and diluted with 800 mL of ethyl acetate. Transfer to a separatory funnel, and repeat washing with 200 mL of deionized water to remove the reaction catalyst and metal impurities. After the obtained solution was concentrated under reduced pressure, 600 mL of ethyl acetate was added to the residue, and the polymer was precipitated with 2,400 mL of hexane. After the precipitated polymer was filtered off and recovered, it was dried under reduced pressure to obtain resin A1 containing a repeating unit represented by the following formula. The Mw of resin A1 is 3,200, and the degree of dispersion (Mw/Mn) is 2.44. Dissolve 20 parts of resin A1, 1 part of acid generator AG, and 4 parts of Nikalac Mw390 (manufactured by Sanwa Chemical Co., Ltd.) as a crosslinking agent in PGMEA containing 0.1% by mass of FC-4430 (manufactured by 3M) 100 parts were filtered with a filter made of a 0.1 μm fluororesin to obtain a resin composition A1. In addition, a composition in which the amount of PGMEA of the resin solution A1 was changed to 35 parts was also prepared in the same manner, and filtered with a filter made of a fluororesin of 0.1 μm to obtain a resin composition A1'.

[Preparation Example 2] In a 1,000 mL flask, 80 g (0.50 mol) of 1,5-dihydroxynaphthalene, 9.0 g (0.30 mol) of paraformaldehyde, and 145 g of methyl serosol were added to the flask. While stirring at 70°C, 20 g of a 20% by mass p-toluenesulfonic acid methyl serosol solution was added. The temperature was increased to 85°C, and after stirring for 6 hours, it was cooled to room temperature and diluted with 800 mL of ethyl acetate. Transfer to a separatory funnel, and repeat washing with 200 mL of deionized water to remove the reaction catalyst and metal impurities. After the obtained solution was concentrated under reduced pressure, 600 mL of ethyl acetate was added to the residue, and the polymer was precipitated with 2,400 mL of hexane. After the precipitated polymer was filtered off and recovered, it was dried under reduced pressure to obtain resin A2 containing a repeating unit represented by the following formula. The Mw of the resin A2 was 1,500, and the Mw/Mn was 2.20. Dissolve 20 parts of resin A2, 1 part of acid generator AG, and 4 parts of Nikalac Mw390 (manufactured by Sanwa Chemical Co., Ltd.) as a crosslinking agent in PGMEA containing 0.1% by mass of FC-4430 (manufactured by 3M) 100 parts were filtered with a filter made of 0.1 μm fluororesin to obtain resin composition A2.

[Preparation Example 3] In a 1,000 mL flask, 72 g (0.50 mol) of 1-hydroxynaphthalene, 51.6 g (0.30 mol) of 2-hydroxy-6-naphthaldehyde and 145 g of methyl serosol were added, While stirring at 70°C, 20 g of a 20% by mass methyl serosulfonate p-toluenesulfonate solution was added. The temperature was increased to 85°C, and after stirring for 6 hours, it was cooled to room temperature and diluted with 800 mL of ethyl acetate. Transfer to a separatory funnel, and repeat washing with 200 mL of deionized water to remove the reaction catalyst and metal impurities. After the obtained solution was concentrated under reduced pressure, 600 mL of ethyl acetate was added to the residue, and the polymer was precipitated with 2,400 mL of hexane. After the precipitated polymer was filtered off and recovered, it was dried under reduced pressure to obtain resin A3 containing a repeating unit represented by the following formula. The Mw of the resin A3 was 2,700, and the Mw/Mn was 2.61. 20 parts of resin A3, 1 part of acid generator AG, and 4 parts of Nikalac Mw390 (manufactured by Sanwa Chemical Co., Ltd.) as a crosslinking agent were dissolved in PGMEA containing 0.1% by mass of FC-4430 (manufactured by 3M) 100 parts were filtered with a filter made of a 0.1 μm fluororesin to obtain a resin composition A3.

[Comparative Preparation Example 1] In a 1,000 mL flask, 32.4 g (0.30 mol) of 2-methylhydroxybenzene, 51.6 g (0.30 mol) of 2-hydroxy-6-naphthaldehyde and methyl sulfonate were added While stirring at 70° C. of 145 g of losu, 20 g of a 20% by mass methyl serosulfate p-toluenesulfonate solution was added. The temperature was increased to 85°C, and after stirring for 6 hours, it was cooled to room temperature and diluted with 800 mL of ethyl acetate. Transfer to a separatory funnel, and repeat washing with 200 mL of deionized water to remove the reaction catalyst and metal impurities. After the obtained solution was concentrated under reduced pressure, 600 mL of ethyl acetate was added to the residue, and the polymer was precipitated with 2,400 mL of hexane. After the precipitated polymer was filtered off and recovered, it was dried under reduced pressure to obtain resin A4 containing a repeating unit represented by the following formula. The Mw of the resin A4 is 2,100, and the Mw/Mn is 1.58. Dissolve 20 parts of resin A4, 1 part of acid generator AG, and 4 parts of Nikalac Mw390 (manufactured by Sanwa Chemical Co., Ltd.) as a crosslinking agent in PGMEA containing 0.1% by mass of FC-4430 (manufactured by 3M) 100 parts were filtered with a 0.1 μm fluororesin filter to obtain resin composition A4.

[Preparation Example 4] Septon 4033, a hydrogenated polystyrene thermoplastic resin manufactured by Kuraray, was made of polystyrene-poly(ethylene/propylene) block-polystyrene copolymer with a styrene content of 30% by mass ) 25g and hydrogenated polystyrene thermoplastic resin Septon 8076 ((stock) Kuraray polystyrene-poly(ethylene/butylene) block-polystyrene copolymer, styrene content 30% by mass) 25g dissolved in homogeneous 150 g of trimethylbenzene, 25% by mass of Septon 4033/8076 mesitylene solution was obtained. The obtained solution was filtered with a 0.2 μm membrane filter to obtain a resin composition B1. In addition, after measuring the glass transition temperature (Tg) of the resin, it was 111°C. [Preparation Example 5] The hydrogenated polystyrene-based thermoplastic resin Septon 4033 ((stock) Kuraray polystyrene-poly(ethylene/propylene) block-polystyrene copolymer, styrene content 30% by mass) ) 25g and hydrogenated polystyrene thermoplastic resin Septon 2002 ((stock) Kuraray polystyrene-poly(ethylene/propylene) block-polystyrene copolymer, styrene content 30% by mass) 25g dissolved in homosan 150 g of toluene, 25% by mass of Septon 4033/2002 mesitylene solution was obtained. The obtained solution was filtered with a 0.2 μm membrane filter to obtain a resin composition B2. Also, after measuring the Tg of the resin, it was 96°C. [Preparation Example 6] Septon 4033, a hydrogenated polystyrene thermoplastic resin manufactured by Kuraray, was made of polystyrene-poly(ethylene/propylene) block-polystyrene copolymer with a styrene content of 30% by mass ) 20g and hydrogenated polystyrene thermoplastic resin Tuftec H1051 (polystyrene-poly(ethylene/butylene) block-polystyrene copolymer manufactured by Asahi Kasei Co., Ltd., styrene content 42% by mass) 20g dissolved In 160 g of mesitylene, a 20% by mass Septon 4033/Tuftec H1051 mesitylene solution was obtained. The resulting solution was filtered with a 0.2 μm membrane filter to obtain a resin composition B3. Also, after measuring the Tg of the resin, it was 101°C. [Comparative Preparation Example 2] The hydrogenated polystyrene-based thermoplastic resin Tuftec H1043 (made by Asahi Kasei Co., Ltd.) was made of polystyrene-poly(ethylene/butylene) block-polystyrene copolymer, styrene Content: 67% by mass) 10 g was dissolved in 190 g of mesitylene to obtain a 5% by mass solution of Tuftec H1043 in mesitylene. The obtained solution was filtered with a 0.2 μm membrane filter to obtain a resin composition B4. Also, after measuring the Tg of the resin, it was 107°C. [0102] Furthermore, the method for measuring the Tg of the resin is as described below. [Method of measuring Tg] The resin compositions B1 to B4 were heated at 180°C for 10 minutes to harden, and a measurement sheet with a thickness of 0.5 mm and a square of 30 mm×10 mm was produced. Using the produced measuring sheet, the dynamic viscoelasticity measuring device (DMA7100 manufactured by Hitachi High-Tech Science) was used to measure at a frequency of 1 Hz and a heating rate of 3°C/min in the range of 0 to 300°C. Take the peak (maximum value) of tanδ as Tg. [0103] [2] Production and evaluation of a wafer laminate [Examples 1 to 6, Comparative Examples 1 to 3] The resin composition A1, A1' was spin-coated on a glass plate with a diameter of 200 mm (thickness: 500 μm) After A2, A3 or A4, heat at 180°C for 2 minutes and 250°C for 5 minutes on a hot plate, so that the material corresponding to the resin layer A is formed into a film with the film thickness shown in Table 1. Further, spin-coated mesitylene solutions B1 and B2 on a 200mm diameter silicon wafer (thickness: 725μm) copper cylinder surface with copper cylinders 10μm high and 40μm in diameter formed on the entire surface, or resin layer A After B3 or B4, heat at 150°C for 5 minutes and 180°C for 5 minutes on a hot plate, thereby forming the thermoplastic resin layer B with the film thickness shown in Table 1. Combination of glass plate-resin layer A and resin layer B-wafer, or glass plate-resin layer A-resin layer B and wafer, with resin surfaces or resin layer B and the copper pillar of the wafer facing each other Method, in a vacuum bonding device (EVG Corporation, EVG520IS), under a reduced pressure of 1 Pa or less, bonding under the conditions shown in Table 1 to produce a wafer laminate. After that, the following test was performed on the bonded substrate. The results are shown in Table 1. Furthermore, the evaluation will be carried out in the following order. [0104] (1) Adhesion test 200mm wafer bonding was performed using EVG's wafer bonding device EVG520IS. The bonding temperature was performed using the values described in Table 1, the pressure in the chamber at the time of bonding was 1 Pa or less, and the load was 20 kN. After joining, cool to room temperature, and confirm the subsequent interface joining conditions with visual inspection and optical microscope. The abnormalities such as bubbles that did not occur at the interface are evaluated as good, which is indicated by "○", and the abnormal conditions are evaluated as Defects are indicated by "×". [0105] (2) Back grinding resistance test A grinding machine (manufactured by DISCO, DAG810) was used to perform back grinding of the silicon wafer using a diamond grindstone. After polishing to a final substrate thickness of 50 μm, an optical microscope (100 times) was used to investigate abnormalities such as cracks and peeling. If there is no abnormality, it is evaluated as good and represented by "○", and the abnormality is evaluated as bad as "×". [0106] (3) CVD resistance test The laminated body after the backside grinding of the silicon wafer was introduced into a CVD apparatus, and a 2 μm SiO ₂ film formation experiment was performed to investigate whether there is an abnormal appearance at this time. If there is no appearance abnormality, it is evaluated as good, and it is indicated by "○", and the appearance abnormality such as porosity, wafer swelling, wafer breakage, etc., is evaluated as bad, and it is indicated by "×". The conditions of the CVD resistance test are as follows. Device name: Plasma CVD PD270STL (manufactured by Samco) RF500W, internal pressure 40Pa TEOS (tetraethylorthosilicate): O ₂ =20sccm:680sccm [0107] (4) Support peelability test Support peeling Sex is evaluated by the following method. First, a dicing frame is used to attach a dicing tape to the wafer side of the wafer laminate whose thickness is reduced to 50 μm after the CVD resistance test is completed, and the surface of the dicing tape is placed on the suction plate by vacuum suction. After that, a 355nm laser was irradiated to the entire surface from the support side. The case where the support and the 50μm wafer can be peeled without breaking is indicated by "○", and the case where abnormality such as cracking occurs is evaluated as defective and indicated by "×". [0108] (5) Washing removability test After the aforementioned peeling test is completed, the following method is used to evaluate the washing and removability test of the solvent. A 200mm wafer (exposed to the CVD resistance test conditions) installed on the dicing frame through the dicing tape, with the resin layer B facing up, is placed on the spin coater, using p-menthane as the cleaning solvent, and spraying for 5 minutes In the cleaning method, isopropyl alcohol (IPA) is sprayed for rinsing while rotating the wafer. After that, the external appearance was observed, and the presence or absence of the remaining resin layer B was visually confirmed. Those with no resin residues are evaluated as good, and those with resin residues as bad are indicated by “×”. [0109] (6) Permeability test The resin composition A1, A1', A2, A3, or A4 was spin-coated on a glass substrate with a thickness of 500 μm to a film thickness of 0.3 μm, and then thermally cured at 250° C. for 5 minutes to form The transmittance (wavelength 355 nm) of the resin layer A was measured using a spectrophotometer (U-4100 model, manufactured by Hitachi High-Tech Science). If the transmittance is less than 20%, it is indicated by "○", and if the transmittance is higher than 20%, it is indicated by "×". [0110] Furthermore, after measuring the transmittance of the resin layer A formed on the support substrate using the resin solutions A1, A1', A2, and A3, it was confirmed that the absorption maximum wavelengths were all 300 to 500 nm. [0111] (7) Measurement of storage modulus The resin compositions B1 to B4 were heated at 180° C. for 10 minutes to harden, and a measurement sheet with a thickness of 0.5 mm and a square of 30 mm×10 mm was produced. Using the produced measuring sheet, the dynamic viscoelasticity measuring device (DMA7100 manufactured by Hitachi High-Tech Science) was used to measure at a frequency of 1 Hz and a heating rate of 3°C/min in the range of 0 to 300°C. The storage modulus is the value at 25°C. [0112] (8) Measurement of tensile breaking strength The resin compositions B1 to B4 were heated at 180° C. for 10 minutes to harden, and a No. 5 dumbbell piece was made from a square sheet with a thickness of 0.4 mm and a 200 mm×40 mm. Using the produced measurement sheet, the tensile tester (V10D manufactured by Toyo Seiki Seisakusho, Ltd.) was used for measurement at a tensile speed of 50 mm/min, and the strength at which the sheet broke was measured as breaking strength (MPa). [0113]

[0114] As shown in Table 1, it can be seen that in Examples 1 to 6, temporary bonding and peeling are easy. On the other hand, in Comparative Example 1, after the laser irradiation, the support did not peel off and cracks occurred. In Comparative Example 2, voids after bonding were confirmed. In Comparative Example 3, cracks occurred after the resin layer B was applied. Furthermore, in Examples 1 to 6, after measuring the surface of the cleaned wafer by the SEM-EDX test, it was confirmed that metal contamination (metal: Ca, K, Na, Mg, Mn, Pb) was a problem Below grade. [0115] In addition, the present invention is not limited to the foregoing embodiment. The foregoing embodiments are just examples, and those having substantially the same constitution as the technical idea described in the scope of the patent application of the present invention and exerting the same effects are all included in the technical scope of the present invention.

[0116]1‧‧‧支持體2‧‧‧接著劑層2a‧‧‧樹脂層A2b‧‧‧樹脂層B3‧‧‧晶圓[0116] 1. ‧ ‧ support body 2. ‧ ‧ adhesive layer 2a ‧ ‧ resin layer A2b ‧ ‧ resin layer B3 ‧ ‧ wafer

[0012] 　　[圖1] 表示本發明之晶圓層合體之一例的示意圖。[0012] 　　 [FIG. 1] A schematic diagram showing an example of the wafer laminate of the present invention.

1‧‧‧支持體 1‧‧‧Support

2‧‧‧接著劑層 2‧‧‧Adhesive layer

2a‧‧‧樹脂層A 2a‧‧‧Resin layer A

2b‧‧‧樹脂層B 2b‧‧‧Resin layer B

3‧‧‧晶圓 3‧‧‧Wafer

Claims

A wafer laminate is a wafer laminate provided with a support, an adhesive layer formed on the support, and a wafer laminated on the adhesive layer with a circuit surface facing the surface , The aforementioned adhesive layer, starting from the aforementioned support side, is composed of a resin layer A with light-shielding properties and a resin layer B containing a non-silicone thermoplastic resin. The resin layer A is composed of resin It is composed of a cured product of substance A, and the resin composition A contains a repeating unit represented by the following formula (1) and a weight average molecular weight of 500 to 500,000 resin A,

(In the formula, R ¹ to R ³ are each independently a hydrogen atom, a hydroxyl group or a monovalent organic group with 1 to 20 carbons, but ^{at least one of R 1} to R ³ is a hydroxyl group; R ⁴ is a hydrogen atom or may A monovalent organic group with a carbon number of 1-30 having a substituent); the resin layer B has a storage modulus E'at 25°C of 1 to 500 MPa, and a tensile breaking strength of 5 to 50 MPa.

Such as the wafer laminate of claim 1, wherein the aforementioned non-silicone-based thermoplastic resin is a resin with a glass transition temperature of -80~120°C.

The wafer laminate described in claim 1 or 2, wherein the wave of the resin layer A The transmittance of 355nm long light is less than 20%.

The wafer laminate of claim 1, wherein the resin composition A further contains a crosslinking agent.

The wafer laminate of claim 1, wherein the resin composition A further contains an acid generator.

The wafer laminate of claim 1, wherein the resin composition A further contains an organic solvent.

A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of claims 1 to 6, comprising (a) a step of directly forming a resin layer A on a support, (b) The step of forming the resin layer B on the circuit formation surface of the wafer, and (c) the step of bonding the resin layer A and the resin layer B under reduced pressure.

A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of claims 1 to 6, comprising (a') directly forming a resin composition for forming a resin layer A on a support The step of layer A', (b) the step of forming the resin layer B on the circuit formation surface of the wafer, (c) the step of bonding the resin composition A'and the resin layer B under reduced pressure, and (d) Perform a step of thermosetting to form the resin layer A and joining.

A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of claims 1 to 6, which includes (a) a step of directly forming a resin layer A on a support, (b') A step of forming a resin layer B on the aforementioned resin layer A, and (c') a step of joining the resin layer B on the aforementioned support to the circuit forming surface of the wafer under reduced pressure.

A method for manufacturing a wafer laminate, which is the method for manufacturing a wafer laminate according to any one of claims 1 to 6, comprising (a') directly forming a resin composition for forming a resin layer A on a support The step of layer A', (b') the step of forming a resin layer B on the resin composition layer A', (c') the resin layer B on the support and the circuit forming surface of the wafer at a reduced pressure The next step of bonding, and (d) the step of thermosetting to form the resin layer A and bonding.

A method for manufacturing a thin wafer, which includes the step of grinding or grinding the circuit non-forming surface of the wafer of the wafer laminate obtained by the method according to any one of claims 7 to 10.